A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721691



Internal ID18673286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34403109..34522329hg38UCSC Ensembl
Innerchr15:34695310..34814530hg19UCSC Ensembl
Innerchr15:32482602..32601822hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38119221
hg19119221
hg18119221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039585
Supporting Variants
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)nssv3721691
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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