A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738250



Internal ID19036531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164260862..164371070hg38UCSC Ensembl
Innerchr3:163978650..164088858hg19UCSC Ensembl
Innerchr3:165461344..165571552hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38110209
hg19110209
hg18110209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008208
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3738250
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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