A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13968228



Internal ID4583470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126969276..127006013hg38UCSC Ensembl
chr10:128767540..128804277hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3836738
hg1936738
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624870
Supporting Variants
SamplesHG04096
Known GenesDOCK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13968228
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