A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13765129



Internal ID3766945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44915494..44919000hg38UCSC Ensembl
chr10:45410942..45414448hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383507
hg193507
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623075
Supporting Variants
SamplesHG03378
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13765129
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