A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679156



Internal ID15415808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9902228..9932098hg38UCSC Ensembl
Innerchr5:9902340..9932210hg19UCSC Ensembl
Innerchr5:9955340..9985210hg18UCSC Ensembl
Innerchr5:9955340..9985210hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3829871
hg1929871
hg1829871
hg1729871
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)nssv679156
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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