A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704062



Internal ID15440714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72812073..72837644hg38UCSC Ensembl
Innerchr9:75426989..75452560hg19UCSC Ensembl
Innerchr9:74616809..74642380hg18UCSC Ensembl
Innerchr9:72656543..72682114hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3825572
hg1925572
hg1825572
hg1725572
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527600
Supporting Variants
Samples
Known GenesTMC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704062
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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