A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1925n106



Internal ID22795753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:62550833..62553965hg38UCSC Ensembl
chr2:62777968..62781100hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129989, nsv1111985, nsv1130225
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1925n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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