A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770450



Internal ID19307116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:3351913..3384434hg38UCSC Ensembl
chr3:3393597..3426118hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3832522
hg1932522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073195
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770450
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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