A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762606



Internal ID18967498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33276993..33277494hg38UCSC Ensembl
chr20:31864799..31865300hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073053
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762606
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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