A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119634



Internal ID19261968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:56365902..56366005hg38UCSC Ensembl
Outerchr20:54940958..54941061hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2269n106
Supporting Variantsnssv3982073
SamplesKWS1
Known GenesFAM210B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119634
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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