A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3536946



Internal ID18835227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20512131hg38UCSC Ensembl
Innerchr15:20216943..20717374hg19UCSC Ensembl
Innerchr15:18476957..18977388hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38500442
hg19500432
hg18500432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041199
Supporting Variants
Samples
Known GenesCHEK2P2, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3536946
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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