A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2607n106



Internal ID22796435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136301758..136307375hg38UCSC Ensembl
chr3:136020600..136026217hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385618
hg195618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1122362, nsv1145460, nsv1119339
SamplesKWS1
Known GenesPCCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2607n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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