A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv97e214



Internal ID20121520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12498443..12508937hg38UCSC Ensembl
chr10:12540442..12550936hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810495
hg1910495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622375, esv3622376
SamplesNA18553
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv97e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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