A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622375



Internal ID6662545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12498443..12507917hg38UCSC Ensembl
Innerchr10:12498443..12507917hg38UCSC Ensembl
Outerchr10:12498243..12507978hg38UCSC Ensembl
chr10:12540442..12549916hg19UCSC Ensembl
Innerchr10:12540442..12549916hg19UCSC Ensembl
Outerchr10:12540242..12549977hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg389475
hg199475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv97e214
Supporting Variantsessv13696590
SamplesNA18553
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622375
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer