A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702833



Internal ID15092799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115982606..115985427hg38UCSC Ensembl
Innerchr5:115318303..115321124hg19UCSC Ensembl
Innerchr5:115346202..115349023hg18UCSC Ensembl
Innerchr5:115346202..115349023hg17UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg382822
hg192822
hg182822
hg172822
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515611
Supporting Variants
Samples
Known GenesAQPEP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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