A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622414



Internal ID6662584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13975258..13992420hg38UCSC Ensembl
Innerchr10:13975269..13992409hg38UCSC Ensembl
Outerchr10:13975247..13992431hg38UCSC Ensembl
chr10:14017258..14034420hg19UCSC Ensembl
Innerchr10:14017269..14034409hg19UCSC Ensembl
Outerchr10:14017247..14034431hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3817163
hg1917163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700542
SamplesHG02153
Known GenesFRMD4A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622414
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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