A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3607952



Internal ID18559547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162464378..162822690hg38UCSC Ensembl
Innerchr3:162182166..162540478hg19UCSC Ensembl
Innerchr3:163664860..164023172hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38358313
hg19358313
hg18358313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012160
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)nssv3607952
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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