A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114068



Internal ID18917868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:36699538..36699590hg38UCSC Ensembl
Outerchr2:36926681..36926733hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973555
SamplesKWS2
Known GenesVIT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114068
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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