A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764649



Internal ID18964253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1312080..1312132hg38UCSC Ensembl
chr20:1292724..1292776hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071671
Supporting Variants
SamplesKWP1
Known GenesFKBP1A-SDCBP2, SDCBP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764649
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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