A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694603



Internal ID15431255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108836409..108837578hg38UCSC Ensembl
Innerchr3:108555256..108556425hg19UCSC Ensembl
Innerchr3:110037946..110039115hg18UCSC Ensembl
Innerchr3:110037946..110039115hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg381170
hg191170
hg181170
hg171170
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521830
Supporting Variants
Samples
Known GenesTRAT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694603
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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