A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3535764



Internal ID18834045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20373156hg38UCSC Ensembl
Innerchr15:20216943..20578409hg19UCSC Ensembl
Innerchr15:18476957..18838423hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38361467
hg19361467
hg18361467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051311
Supporting Variants
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3535764
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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