A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622385



Internal ID6662555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12746084..12756145hg38UCSC Ensembl
Innerchr10:12746123..12756106hg38UCSC Ensembl
Outerchr10:12746045..12756184hg38UCSC Ensembl
chr10:12788083..12798144hg19UCSC Ensembl
Innerchr10:12788122..12798105hg19UCSC Ensembl
Outerchr10:12788044..12798183hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3810062
hg1910062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13697723
SamplesHG04035
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622385
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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