A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2271n106



Internal ID22796099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57117544..57118344hg38UCSC Ensembl
chr20:55692600..55693400hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126598, nsv1136330
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2271n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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