A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696153



Internal ID15086119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2623904..2633432hg38UCSC Ensembl
Innerchr7:2663538..2673066hg19UCSC Ensembl
Innerchr7:2630064..2639592hg18UCSC Ensembl
Innerchr7:2436779..2446307hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg389529
hg199529
hg189529
hg179529
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517403
Supporting Variants
Samples
Known GenesTTYH3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696153
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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