A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008585



Internal ID19097802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50897597..50917987hg38UCSC Ensembl
Innerchr3:50935028..50955418hg19UCSC Ensembl
Innerchr3:50903785..50930443hg18UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3820391
hg1920391
hg1826659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3595256
Samples
Known GenesDOCK3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008585
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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