A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv479n106



Internal ID20159836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73873642..73874842hg38UCSC Ensembl
chr10:75633400..75634600hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121816, nsv1143510
SamplesKWS1, KWS2
Known GenesCAMK2G
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv479n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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