A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039548



Internal ID19128767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54564767..54622321hg38UCSC Ensembl
Innerchr15:54856965..54914519hg19UCSC Ensembl
Innerchr15:52644257..52701811hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3857555
hg1957555
hg1857555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552436
Samples
Known GenesUNC13C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039548
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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