A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965584



Internal ID18884863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:38895828..38895957hg38UCSC Ensembl
Outerchr20:37524471..37524600hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121579
Supporting Variants
SamplesKWS2
Known GenesPPP1R16B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965584
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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