A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762789



Internal ID19308596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61995464..61995882hg38UCSC Ensembl
chr20:60570520..60570938hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073077
Supporting Variants
SamplesKWP1
Known GenesTAF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762789
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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