A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624782



Internal ID7011632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122602807..122624657hg38UCSC Ensembl
chr10:124362323..124384173hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3821851
hg1921851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13956580
SamplesNA19041
Known GenesDMBT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624782
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