A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120876



Internal ID19274586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:157071627..157074857hg38UCSC Ensembl
Outerchr5:156498638..156501868hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383231
hg193231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3202n106
Supporting Variantsnssv3963324
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120876
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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