A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150337



Internal ID19196098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:83300537..83300835hg38UCSC Ensembl
Outerchr4:84221690..84221988hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003637
SamplesKWB1
Known GenesHPSE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150337
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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