A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770131



Internal ID18967493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:142723857..142724258hg38UCSC Ensembl
chr3:142442699..142443100hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073252
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770131
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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