A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063707



Internal ID18806238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46147167..46205998hg38UCSC Ensembl
Innerchr17:44224533..44283364hg19UCSC Ensembl
Innerchr17:41580310..41639141hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3858832
hg1958832
hg1858832
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3221n100
Supporting Variantsnssv3556843, nssv3556844, nssv3724179, nssv3724180
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)nsv1063707
Frequency
Sample Size29084
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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