A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2690n106



Internal ID22796518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197032584..197034809hg38UCSC Ensembl
chr3:196759455..196761680hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg382226
hg192226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1140174, nsv1129242
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2690n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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