A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528263



Internal ID15108870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16194116..16293682hg38UCSC Ensembl
Innerchr17:16097430..16196996hg19UCSC Ensembl
Innerchr17:16038155..16137721hg18UCSC Ensembl
Innerchr17:16038155..16137721hg17UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3899567
hg1999567
hg1899567
hg1799567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704830
Samples
Known GenesMIR1288, NCOR1, PIGL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528263
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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