A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699827



Internal ID15436479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135258185..135260498hg38UCSC Ensembl
Innerchr7:134942937..134945250hg19UCSC Ensembl
Innerchr7:134593477..134595790hg18UCSC Ensembl
Innerchr7:134400192..134402505hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382314
hg192314
hg182314
hg172314
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523974
Supporting Variants
Samples
Known GenesSTRA8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699827
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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