A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3793n106



Internal ID22797621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21767188..21804588hg38UCSC Ensembl
chr8:21624700..21662100hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3837401
hg1937401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126849, nsv1137612
SamplesKWS2, KWS1
Known GenesGFRA2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3793n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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