A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13890402



Internal ID4182571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88791335..88872446hg38UCSC Ensembl
chr10:90551092..90632203hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3881112
hg1981112
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624140
Supporting Variants
SamplesHG03777
Known GenesANKRD22, LIPM
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13890402
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