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nsv4209212

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:69,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 13 studies. See in: genome view    
Remapped(Score: Perfect):69,533,220-69,602,220Question Mark
Overlapping variant regions from other studies: 85 SVs from 13 studies. See in: genome view    
Submitted genomic69,927,000-69,996,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4209212RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1269,533,22069,602,220
nsv4209212Submitted genomicGRCh37.p13Primary AssemblyNC_000012.11Chr1269,927,00069,996,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15948658duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15948658RemappedPerfectNC_000012.12:g.695
33220_69602220dup
GRCh38.p12First PassNC_000012.12Chr1269,533,22069,602,220
nssv15948658Submitted genomicNC_000012.11:g.699
27000_69996000dup
GRCh37.p13NC_000012.11Chr1269,927,00069,996,000

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv159486584.6e-005121676
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