A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128190



Internal ID18909805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133066688..133066738hg38UCSC Ensembl
Outerchr5:132402380..132402430hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957677
SamplesKWS1
Known GenesHSPA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128190
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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