A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690488



Internal ID1175529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9186116..9189227hg38UCSC Ensembl
Innerchr10:9186126..9189217hg38UCSC Ensembl
Outerchr10:9186106..9189237hg38UCSC Ensembl
chr10:9228079..9231190hg19UCSC Ensembl
Innerchr10:9228089..9231180hg19UCSC Ensembl
Outerchr10:9228069..9231200hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383112
hg193112
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622302
Supporting Variants
SamplesHG01055
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690488
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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