A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697133



Internal ID15433785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:61413920..61437100hg38UCSC Ensembl
Innerchr17:59491281..59514461hg19UCSC Ensembl
Innerchr17:56846063..56869243hg18UCSC Ensembl
Innerchr17:56846063..56869243hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3823181
hg1923181
hg1823181
hg1723181
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519931
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697133
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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