A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622408



Internal ID6662578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13689064..13692594hg38UCSC Ensembl
Innerchr10:13689064..13692594hg38UCSC Ensembl
Outerchr10:13688909..13692701hg38UCSC Ensembl
chr10:13731064..13734594hg19UCSC Ensembl
Innerchr10:13731064..13734594hg19UCSC Ensembl
Outerchr10:13730909..13734701hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383531
hg193531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700530
SamplesHG02439
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622408
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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