A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688090



Internal ID15424742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902228..9924060hg38UCSC Ensembl
Innerchr5:9902340..9924172hg19UCSC Ensembl
Innerchr5:9955340..9977172hg18UCSC Ensembl
Innerchr5:9955340..9977172hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3821833
hg1921833
hg1821833
hg1721833
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517239
Supporting Variants
Samples
Known GenesLOC285692
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688090
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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