A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151982



Internal ID18849295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:45023988..45024049hg38UCSC Ensembl
Outerchr19:45527246..45527307hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999163
SamplesKWB1
Known GenesRELB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151982
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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