A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063151



Internal ID18805682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46135838..46169798hg38UCSC Ensembl
Innerchr17:44213204..44247164hg19UCSC Ensembl
Innerchr17:41568981..41602941hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3833961
hg1933961
hg1833961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3212n100
Supporting Variantsnssv3550066, nssv3550065
Samples
Known GenesKANSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063151
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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