A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119039



Internal ID18916044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:138352611..138353111hg38UCSC Ensembl
Outerchr5:137688300..137688800hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3180n106
Supporting Variantsnssv3981836
SamplesKWS1
Known GenesKDM3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119039
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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