A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762195



Internal ID18962343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37187267..37187520hg38UCSC Ensembl
chr20:35815670..35815923hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071694
Supporting Variants
SamplesKWP1
Known GenesRPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762195
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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