A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700710



Internal ID15090676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:116063479..116063649hg38UCSC Ensembl
Innerchr5:115399176..115399346hg19UCSC Ensembl
Innerchr5:115427075..115427245hg18UCSC Ensembl
Innerchr5:115427075..115427245hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38171
hg19171
hg18171
hg17171
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515611
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700710
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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