A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061170



Internal ID18803701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46120237..46186703hg38UCSC Ensembl
Innerchr17:44197603..44264069hg19UCSC Ensembl
Innerchr17:41553381..41619846hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3866467
hg1966467
hg1866466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3199n100
Supporting Variantsnssv3549807, nssv3720640, nssv3549803, nssv3549806, nssv3549804, nssv3549805
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)nsv1061170
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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