A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622409



Internal ID6662579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13730148..13732292hg38UCSC Ensembl
Innerchr10:13730159..13732281hg38UCSC Ensembl
Outerchr10:13730137..13732303hg38UCSC Ensembl
chr10:13772148..13774292hg19UCSC Ensembl
Innerchr10:13772159..13774281hg19UCSC Ensembl
Outerchr10:13772137..13774303hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382145
hg192145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700531
SamplesHG02890
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622409
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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