A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2372n106



Internal ID20161729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25990736..25990800hg38UCSC Ensembl
chr21:27363050..27363114hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1136615, nsv1127890
SamplesKWS1, KWS2
Known GenesAPP
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2372n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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