A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739706



Internal ID19037987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41317573..41782346hg38UCSC Ensembl
Innerchr3:41359064..41823838hg19UCSC Ensembl
Innerchr3:41334068..41798842hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38464774
hg19464775
hg18464775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001928
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)nssv3739706
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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