A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659489



Internal ID15396141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111404915..111472797hg38UCSC Ensembl
Innerchr7:111044971..111112853hg19UCSC Ensembl
Innerchr7:110832207..110900089hg18UCSC Ensembl
Innerchr7:110638922..110706804hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3867883
hg1967883
hg1867883
hg1767883
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659489
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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