A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701402



Internal ID15438054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126614957..126621111hg38UCSC Ensembl
Innerchr3:126333800..126339954hg19UCSC Ensembl
Innerchr3:127816490..127822644hg18UCSC Ensembl
Innerchr3:127816498..127822652hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386155
hg196155
hg186155
hg176155
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525296
Supporting Variants
Samples
Known GenesTXNRD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701402
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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