A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13737819



Internal ID3739635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28153218..28157119hg38UCSC Ensembl
Innerchr10:28153368..28156969hg38UCSC Ensembl
Outerchr10:28153068..28157269hg38UCSC Ensembl
chr10:28442147..28446048hg19UCSC Ensembl
Innerchr10:28442297..28445898hg19UCSC Ensembl
Outerchr10:28441997..28446198hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg383902
hg193902
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622739
Supporting Variants
SamplesHG01948
Known GenesMPP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13737819
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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