A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686682



Internal ID15423334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:129664053..129776411hg38UCSC Ensembl
Innerchr3:129382896..129495254hg19UCSC Ensembl
Innerchr3:130865586..130977944hg18UCSC Ensembl
Innerchr3:130865594..130977952hg17UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38112359
hg19112359
hg18112359
hg17112359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516538
Supporting Variants
Samples
Known GenesTMCC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686682
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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