A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040216



Internal ID18782747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:53451583..53559482hg38UCSC Ensembl
Innerchr15:53743780..53851679hg19UCSC Ensembl
Innerchr15:51531072..51638971hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38107900
hg19107900
hg18107900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552421
Samples
Known GenesWDR72
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040216
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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