A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147961



Internal ID18852633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:35045712..35045790hg38UCSC Ensembl
Outerchr19:35536616..35536694hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001470
SamplesKWB1
Known GenesHPN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147961
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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