A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061056



Internal ID19150275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19591492..19631681hg38UCSC Ensembl
Innerchr17:19494805..19534994hg19UCSC Ensembl
Innerchr17:19435397..19475586hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3840190
hg1940190
hg1840190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3117n100
Supporting Variantsnssv3560541
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)nsv1061056
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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