A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv391n106



Internal ID20159748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32024299..32024368hg38UCSC Ensembl
chr10:32313227..32313296hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1145437, nsv1113264
SamplesKWS2, KWS1
Known GenesKIF5B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv391n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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