A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670765



Internal ID15407417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97714396..97745816hg38UCSC Ensembl
Innerchr5:97050100..97081520hg19UCSC Ensembl
Innerchr5:97075856..97107276hg18UCSC Ensembl
Innerchr5:97075856..97107276hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3831421
hg1931421
hg1831421
hg1731421
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517188
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670765
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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