A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622959



Internal ID6663128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37442414..37747570hg38UCSC Ensembl
chr10:37731342..38036498hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38305157
hg19305157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv112e214
Supporting Variantsessv13756806
SamplesHG00473
Known GenesMTRNR2L7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622959
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