A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv218n106



Internal ID22794046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165761972..165762255hg38UCSC Ensembl
chr1:165731209..165731492hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120618, nsv1135392
SamplesKWS2
Known GenesTMCO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv218n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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