A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704129



Internal ID15440781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111192780..111649911hg38UCSC Ensembl
Innerchr7:110832836..111289967hg19UCSC Ensembl
Innerchr7:110620072..111077203hg18UCSC Ensembl
Innerchr7:110426787..110883918hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38457132
hg19457132
hg18457132
hg17457132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527658
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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