A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664710



Internal ID3666526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1235181..1241508hg38UCSC Ensembl
Innerchr10:1235203..1241487hg38UCSC Ensembl
Outerchr10:1235160..1241530hg38UCSC Ensembl
chr10:1281117..1283571hg19UCSC Ensembl
Innerchr10:1281139..1283550hg19UCSC Ensembl
Outerchr10:1281096..1283593hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg386328
hg192455
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622099
Supporting Variants
SamplesHG01980
Known GenesADARB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664710
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