A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623816



Internal ID7010672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73606004..73608789hg38UCSC Ensembl
Innerchr10:73606043..73608751hg38UCSC Ensembl
Outerchr10:73605966..73608828hg38UCSC Ensembl
chr10:75365762..75368547hg19UCSC Ensembl
Innerchr10:75365801..75368509hg19UCSC Ensembl
Outerchr10:75365724..75368586hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861917, essv13861918
SamplesNA19917, NA18511
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623816
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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