A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972924



Internal ID19241231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:33502584..33502650hg38UCSC Ensembl
Outerchr20:32090390..32090456hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136537
Supporting Variants
SamplesKWS2
Known GenesCBFA2T2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972924
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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