A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143979



Internal ID19287069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:20827657..20828257hg38UCSC Ensembl
Outerchr20:20808300..20808900hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994691
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143979
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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