A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv62n106



Internal ID20159419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24162714..24162778hg38UCSC Ensembl
chr1:24489204..24489268hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1133823, nsv1126982
SamplesKWS2, KWS1
Known GenesIFNLR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv62n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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