A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv67n106



Internal ID19018176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26695709..26698009hg38UCSC Ensembl
chr1:27022200..27024500hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126186, nsv1121758
SamplesKWS1, KWS2
Known GenesARID1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv67n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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