A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4139n106



Internal ID20163496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126326621..126327221hg38UCSC Ensembl
chr9:129088900..129089500hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1113015, nsv1145264
SamplesKWS2, KWS1
Known GenesMVB12B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4139n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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