A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545646



Internal ID18843927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27666188..27682648hg38UCSC Ensembl
Innerchr15:27911334..27927794hg19UCSC Ensembl
Innerchr15:25584929..25601389hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3816461
hg1916461
hg1816461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042028
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3545646
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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