A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528785



Internal ID15456078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:62877363..62892145hg38UCSC Ensembl
Innerchr17:60954724..60969506hg19UCSC Ensembl
Innerchr17:58308456..58323238hg18UCSC Ensembl
Innerchr17:58308456..58323238hg17UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3814783
hg1914783
hg1814783
hg1714783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705452
Samples
Known GenesMIR548W
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528785
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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