A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149059



Internal ID18852396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35106036..35106127hg38UCSC Ensembl
Outerchr19:35596940..35597031hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002569
SamplesKWB1
Known GenesHPN-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149059
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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