A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622403



Internal ID7009262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13403502..13412536hg38UCSC Ensembl
Innerchr10:13403502..13412536hg38UCSC Ensembl
Outerchr10:13403210..13412834hg38UCSC Ensembl
chr10:13445502..13454536hg19UCSC Ensembl
Innerchr10:13445502..13454536hg19UCSC Ensembl
Outerchr10:13445210..13454834hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg389035
hg199035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700172, essv13700173, essv13700174
SamplesHG02384, HG02345, HG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622403
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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