A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv89n106



Internal ID22793917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56422030..56422347hg38UCSC Ensembl
chr1:56887702..56888019hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120609, nsv1137764
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv89n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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