A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763721



Internal ID19307006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191761673..191763174hg38UCSC Ensembl
chr2:192626399..192627900hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072473
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763721
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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