A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131751



Internal ID18933170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:190845696..190845760hg38UCSC Ensembl
Outerchr3:190563485..190563549hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986284
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131751
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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