A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524934



Internal ID15105541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26515120..26649934hg38UCSC Ensembl
Innerchr15:26760267..26895081hg19UCSC Ensembl
Innerchr15:24311360..24446174hg18UCSC Ensembl
Innerchr15:24311360..24446174hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38134815
hg19134815
hg18134815
hg17134815
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv144n21
Supporting Variantsnssv700947
Samples
Known GenesGABRB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524934
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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