A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13785621



Internal ID3787437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46224802..46263254hg38UCSC Ensembl
chr10:47596038..47634490hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3838453
hg1938453
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623128
Supporting Variants
SamplesNA18504
Known GenesANTXRLP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13785621
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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