A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074657



Internal ID19323225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197032404..197032763hg38UCSC Ensembl
chr3:196759275..196759634hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769838
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074657
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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