A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065192



Internal ID18807723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46135050..46205998hg38UCSC Ensembl
Innerchr17:44212416..44283364hg19UCSC Ensembl
Innerchr17:41568193..41639141hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3870949
hg1970949
hg1870949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3216n100
Supporting Variantsnssv3718452, nssv3718453
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)nsv1065192
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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