A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053870



Internal ID18796401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34421910..34520906hg38UCSC Ensembl
Innerchr15:34714111..34813107hg19UCSC Ensembl
Innerchr15:32501403..32600399hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3898997
hg1998997
hg1898997
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2562n100
Supporting Variantsnssv3548907, nssv3548905, nssv3548904, nssv3548903, nssv3548906
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053870
Frequency
Sample Size29084
Observed Gain1
Observed Loss4
Observed Complex0
Frequencyn/a


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