A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699914



Internal ID15089880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84864333..84935498hg38UCSC Ensembl
Innerchr15:85407564..85478729hg19UCSC Ensembl
Innerchr15:83208568..83279733hg18UCSC Ensembl
Innerchr15:83208568..83279733hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3871166
hg1971166
hg1871166
hg1771166
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524050
Supporting Variants
Samples
Known GenesALPK3, SLC28A1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699914
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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