A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv98n106



Internal ID22793926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66423062..66440117hg38UCSC Ensembl
chr1:66888745..66905800hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3817056
hg1917056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111771, nsv1135391
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv98n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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