A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109732



Internal ID18915712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:141667580..141667637hg38UCSC Ensembl
Outerchr5:141047147..141047204hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958068
SamplesKWS1
Known GenesARAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109732
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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