A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516802



Internal ID15444095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:26964359..26965827hg38UCSC Ensembl
Innerchr13:27538496..27539964hg19UCSC Ensembl
Innerchr13:26436496..26437964hg18UCSC Ensembl
Innerchr13:26436496..26437964hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381469
hg191469
hg181469
hg171469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671015, nssv663608
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516802
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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