A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062691



Internal ID18805222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46113306..46186703hg38UCSC Ensembl
Innerchr17:44190672..44264069hg19UCSC Ensembl
Innerchr17:41546454..41619846hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3873398
hg1973398
hg1873393
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3201n100
Supporting Variantsnssv3548623, nssv3548622
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)nsv1062691
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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