A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144937



Internal ID19265480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44810159..44810759hg38UCSC Ensembl
Outerchr20:43438800..43439400hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981546
SamplesKWS1
Known GenesRIMS4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144937
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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