A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1264n54



Internal ID20134688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73873821..73874904hg38UCSC Ensembl
chr10:75633579..75634662hg19UCSC Ensembl
chr10:75303585..75304668hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381084
hg191084
hg181084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551520, nsv551525, nsv551524, nsv551522, nsv551519
Samples
Known GenesCAMK2G
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1264n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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