A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13714415



Internal ID1322003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20722323..20724561hg38UCSC Ensembl
Innerchr10:20722360..20724525hg38UCSC Ensembl
Outerchr10:20722287..20724598hg38UCSC Ensembl
chr10:21011252..21013490hg19UCSC Ensembl
Innerchr10:21011289..21013454hg19UCSC Ensembl
Outerchr10:21011216..21013527hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382239
hg192239
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622563
Supporting Variants
SamplesHG01168
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13714415
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer