A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697255



Internal ID15087221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58319248..58344345hg38UCSC Ensembl
Innerchr17:56396609..56421706hg19UCSC Ensembl
Innerchr17:53751608..53776705hg18UCSC Ensembl
Innerchr17:53751608..53776705hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3825098
hg1925098
hg1825098
hg1725098
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517229
Supporting Variants
Samples
Known GenesBZRAP1, BZRAP1-AS1, MIR142, MIR4736
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697255
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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