A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059047



Internal ID19148266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6203793..6230674hg38UCSC Ensembl
Innerchr17:6107113..6133994hg19UCSC Ensembl
Innerchr17:6047837..6074718hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3826882
hg1926882
hg1826882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3091n100
Supporting Variantsnssv3560299
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059047
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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