A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700838



Internal ID15090804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58316353..58324223hg38UCSC Ensembl
Innerchr17:56393714..56401584hg19UCSC Ensembl
Innerchr17:53748713..53756583hg18UCSC Ensembl
Innerchr17:53748713..53756583hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg387871
hg197871
hg187871
hg177871
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517229
Supporting Variants
Samples
Known GenesBZRAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700838
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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