A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902085



Internal ID3903901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94643661..94761810hg38UCSC Ensembl
Innerchr10:94643670..94761802hg38UCSC Ensembl
Outerchr10:94643653..94761819hg38UCSC Ensembl
chr10:96403418..96521567hg19UCSC Ensembl
Innerchr10:96403427..96521559hg19UCSC Ensembl
Outerchr10:96403410..96521576hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38118150
hg19118150
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624253
Supporting Variants
SamplesHG00185
Known GenesCYP2C18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902085
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