A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589692



Internal ID18541287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39051835..39094306hg38UCSC Ensembl
Innerchr3:39093326..39135797hg19UCSC Ensembl
Innerchr3:39068330..39110801hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3842472
hg1942472
hg1842472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007100
Supporting Variants
Samples
Known GenesWDR48
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589692
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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