A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622407



Internal ID6662577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13680845..13682023hg38UCSC Ensembl
Innerchr10:13680869..13681999hg38UCSC Ensembl
Outerchr10:13680821..13682047hg38UCSC Ensembl
chr10:13722845..13724023hg19UCSC Ensembl
Innerchr10:13722869..13723999hg19UCSC Ensembl
Outerchr10:13722821..13724047hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700529
SamplesHG00451
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622407
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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