A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136727



Internal ID18926044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:58509667..58509731hg38UCSC Ensembl
Outerchr3:58495394..58495458hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973122
SamplesKWS2
Known GenesACOX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136727
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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