A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv368n106



Internal ID20159725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13115031..13115106hg38UCSC Ensembl
chr10:13157031..13157106hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1137877, nsv1145432
SamplesKWS1, KWS2
Known GenesOPTN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv368n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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