A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061086



Internal ID19150305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46099606..46284631hg38UCSC Ensembl
Innerchr17:44176972..44361997hg19UCSC Ensembl
Innerchr17:41532785..41717774hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38185026
hg19185026
hg18184990
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3181n100
Supporting Variantsnssv3548466, nssv3548465
Samples
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061086
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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