A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv328n106



Internal ID20159685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:134760..136060hg38UCSC Ensembl
chr10:180700..182000hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112569, nsv1143485
SamplesKWS2, KWS1
Known GenesZMYND11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv328n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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