A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055651



Internal ID19144870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46144772..46209238hg38UCSC Ensembl
Innerchr17:44222138..44286604hg19UCSC Ensembl
Innerchr17:41577915..41642381hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3864467
hg1964467
hg1864467
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3213n100
Supporting Variantsnssv3556779, nssv3724128, nssv3724129, nssv3556780
Samples
Known GenesKANSL1, KANSL1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055651
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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