A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5587422



Internal ID8564825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12558554..12560556hg38UCSC Ensembl
chr10:12600553..12602555hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382003
hg192003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675595
Supporting Variants
SamplesNA19394
Known GenesCAMK1D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5587422
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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