A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4021n106



Internal ID22797849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67677963..67683961hg38UCSC Ensembl
chr9:46343800..46349800hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385999
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1133721, nsv1144266
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4021n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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