A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764887



Internal ID18964751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2591341..2591663hg38UCSC Ensembl
chr3:2633025..2633347hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071854
Supporting Variants
SamplesKWP1
Known GenesCNTN4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764887
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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