A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763680



Internal ID18959875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48827562..48828263hg38UCSC Ensembl
chr20:47444099..47444800hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072543
Supporting Variants
SamplesKWP1
Known GenesPREX1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763680
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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