A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4125n106



Internal ID20163482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111483420..111484420hg38UCSC Ensembl
chr9:114245700..114246700hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1119605, nsv1133739
SamplesKWS1, KWS2
Known GenesKIAA0368
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4125n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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