A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3555188



Internal ID18853469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87353751..87370306hg38UCSC Ensembl
Innerchr15:87896982..87913537hg19UCSC Ensembl
Innerchr15:85697986..85714541hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3816556
hg1916556
hg1816556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047161
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)nssv3555188
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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