A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614538



Internal ID18912819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164243312..164681437hg38UCSC Ensembl
Innerchr3:163961100..164399225hg19UCSC Ensembl
Innerchr3:165443794..165881919hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38438126
hg19438126
hg18438126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010490
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)nssv3614538
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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