A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109381



Internal ID19265699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:50851078..50851129hg38UCSC Ensembl
Outerchr20:49467615..49467666hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956069
SamplesKWS1
Known GenesBCAS4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109381
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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