A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663804



Internal ID15400456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902291..9924060hg38UCSC Ensembl
Innerchr5:9902403..9924172hg19UCSC Ensembl
Innerchr5:9955403..9977172hg18UCSC Ensembl
Innerchr5:9955403..9977172hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3821770
hg1921770
hg1821770
hg1721770
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)nssv663804
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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