A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109698



Internal ID18901091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:55860307..55860367hg38UCSC Ensembl
Outerchr5:55156135..55156195hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957270
SamplesKWS1
Known GenesIL31RA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109698
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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