A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13861545



Internal ID511204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71939403..71946160hg38UCSC Ensembl
Innerchr10:71939403..71946160hg38UCSC Ensembl
Outerchr10:71939236..71946615hg38UCSC Ensembl
chr10:73699161..73705918hg19UCSC Ensembl
Innerchr10:73699161..73705918hg19UCSC Ensembl
Outerchr10:73698994..73706373hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386758
hg196758
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623785
Supporting Variants
SamplesHG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13861545
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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