A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704852



Internal ID15441504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:92688925..92704514hg38UCSC Ensembl
Innerchr5:92024632..92040221hg19UCSC Ensembl
Innerchr5:92050388..92065977hg18UCSC Ensembl
Innerchr5:92050388..92065977hg17UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3815590
hg1915590
hg1815590
hg1715590
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528282
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704852
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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