A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2387n106



Internal ID19020496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38528422..38528746hg38UCSC Ensembl
chr21:39900346..39900670hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120791, nsv1119697, nsv1121245
SamplesKWS1, KWS2
Known GenesERG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2387n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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