A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589706



Internal ID18887987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41317573..41782940hg38UCSC Ensembl
Innerchr3:41359064..41824432hg19UCSC Ensembl
Innerchr3:41334068..41799436hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38465368
hg19465369
hg18465369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012443
Supporting Variants
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589706
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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