A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136253



Internal ID18922106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:57435368..57436168hg38UCSC Ensembl
Outerchr18:55102600..55103400hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1614n106
Supporting Variantsnssv3989867
SamplesKWS2
Known GenesONECUT2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136253
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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