A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4127n106



Internal ID20163484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112502365..112502457hg38UCSC Ensembl
chr9:115264645..115264737hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135743, nsv1132077
SamplesKWS1, KWS2
Known GenesKIAA1958
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4127n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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