A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705947



Internal ID15442599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15689448..15704880hg38UCSC Ensembl
Innerchr17:15592762..15608194hg19UCSC Ensembl
Innerchr17:15533487..15548919hg18UCSC Ensembl
Innerchr17:15533487..15548919hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3815433
hg1915433
hg1815433
hg1715433
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522564
Supporting Variants
Samples
Known GenesZNF286A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705947
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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