A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073683



Internal ID19325333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139114457..139116158hg38UCSC Ensembl
chr3:138833299..138835000hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381702
hg191702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771968
SamplesKWP1
Known GenesBPESC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073683
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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