A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1909n106



Internal ID22795737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:51070139..51156062hg38UCSC Ensembl
chr2:51297277..51383200hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3885924
hg1985924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111805, nsv1120749
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1909n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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