A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696641



Internal ID15433293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:194617172..194619255hg38UCSC Ensembl
Innerchr3:194337901..194339984hg19UCSC Ensembl
Innerchr3:195819190..195821273hg18UCSC Ensembl
Innerchr3:195819198..195821281hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382084
hg192084
hg182084
hg172084
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517166
Supporting Variants
Samples
Known GenesTMEM44
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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