A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13837749



Internal ID1713425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64912093..64950564hg38UCSC Ensembl
chr10:66671851..66710322hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3838472
hg1938472
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623546
Supporting Variants
SamplesHG01596
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13837749
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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