A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13680540



Internal ID1864606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3745682..3746494hg38UCSC Ensembl
Innerchr10:3745743..3746433hg38UCSC Ensembl
Outerchr10:3745621..3746555hg38UCSC Ensembl
chr10:3787874..3788686hg19UCSC Ensembl
Innerchr10:3787935..3788625hg19UCSC Ensembl
Outerchr10:3787813..3788747hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622182
Supporting Variants
SamplesHG01765
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13680540
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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