A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062876



Internal ID19152095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46135838..46218456hg38UCSC Ensembl
Innerchr17:44213204..44295822hg19UCSC Ensembl
Innerchr17:41568981..41651599hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3882619
hg1982619
hg1882619
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3213n100
Supporting Variantsnssv3550084, nssv3550085, nssv3550083
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)nsv1062876
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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