A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv112e214



Internal ID20121535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:37441894..37765337hg38UCSC Ensembl
chr10:37730822..38054265hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38323444
hg19323444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622959, esv3622958
SamplesHG00473
Known GenesMTRNR2L7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv112e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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