A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv931n106



Internal ID20160288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:24696408..24696790hg38UCSC Ensembl
chr13:25270546..25270928hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135002, nsv1111904
SamplesKWS2
Known GenesATP12A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv931n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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