A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059150



Internal ID18801681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46120237..46192180hg38UCSC Ensembl
Innerchr17:44197603..44269546hg19UCSC Ensembl
Innerchr17:41553381..41625323hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3871944
hg1971944
hg1871943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3199n100
Supporting Variantsnssv3549809
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)nsv1059150
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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