A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13864476



Internal ID3866292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76130938..76133075hg38UCSC Ensembl
Innerchr10:76130938..76133075hg38UCSC Ensembl
Outerchr10:76130876..76133115hg38UCSC Ensembl
chr10:77890696..77892833hg19UCSC Ensembl
Innerchr10:77890696..77892833hg19UCSC Ensembl
Outerchr10:77890634..77892873hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382138
hg192138
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623860
Supporting Variants
SamplesHG02048
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13864476
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