A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151620



Internal ID18853737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:33057097..33057262hg38UCSC Ensembl
Outerchr2:33282164..33282329hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003040
SamplesKWB1
Known GenesLTBP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151620
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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