A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153052



Internal ID19197916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:17745296..17745952hg38UCSC Ensembl
Outerchr19:17856105..17856761hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998084
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153052
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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