A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3225n106



Internal ID22797053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175918297..175941297hg38UCSC Ensembl
chr5:175345300..175368300hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3823001
hg1923001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1118740, nsv1115708
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3225n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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