A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13737567



Internal ID3739383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27694908..27707715hg38UCSC Ensembl
Innerchr10:27694958..27707665hg38UCSC Ensembl
Outerchr10:27694836..27707787hg38UCSC Ensembl
chr10:27983837..27996644hg19UCSC Ensembl
Innerchr10:27983887..27996594hg19UCSC Ensembl
Outerchr10:27983765..27996716hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3812808
hg1912808
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622732
Supporting Variants
SamplesNA20772
Known GenesMKX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13737567
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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