A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062065



Internal ID18804596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46120237..46164298hg38UCSC Ensembl
Innerchr17:44197603..44241664hg19UCSC Ensembl
Innerchr17:41553381..41597441hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3844062
hg1944062
hg1844061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3205n100
Supporting Variantsnssv3549796, nssv3549794, nssv3549795
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)nsv1062065
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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