A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701565



Internal ID15438217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81580540..81668633hg38UCSC Ensembl
Innerchr5:80876359..80964452hg19UCSC Ensembl
Innerchr5:80912115..81000208hg18UCSC Ensembl
Innerchr5:80912115..81000208hg17UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3888094
hg1988094
hg1888094
hg1788094
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525437
Supporting Variants
Samples
Known GenesSSBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701565
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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