A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063363



Internal ID19152582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46135838..46190269hg38UCSC Ensembl
Innerchr17:44213204..44267635hg19UCSC Ensembl
Innerchr17:41568981..41623412hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3854432
hg1954432
hg1854432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3217n100
Supporting Variantsnssv3550070
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)nsv1063363
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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