A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059575



Internal ID19148794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:52878097..53237046hg38UCSC Ensembl
Innerchr17:50955457..51314407hg19UCSC Ensembl
Innerchr17:48310456..48669406hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38358950
hg19358951
hg18358951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3264n100
Supporting Variantsnssv3566098
Samples
Known GenesC17orf112
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059575
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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