A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622687



Internal ID7009545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26171089..26176292hg38UCSC Ensembl
Innerchr10:26171089..26176292hg38UCSC Ensembl
Outerchr10:26170810..26176490hg38UCSC Ensembl
chr10:26460018..26465221hg19UCSC Ensembl
Innerchr10:26460018..26465221hg19UCSC Ensembl
Outerchr10:26459739..26465419hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385204
hg195204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13728471, essv13728470
SamplesHG01369, HG00182
Known GenesMYO3A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622687
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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