A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545665



Internal ID18497260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28110984..28193879hg38UCSC Ensembl
Innerchr15:28356130..28439025hg19UCSC Ensembl
Innerchr15:26029725..26112620hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3882896
hg1982896
hg1882896
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036445
Supporting Variants
Samples
Known GenesHERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545665
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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