A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13953790



Internal ID4843608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121674875..121703457hg38UCSC Ensembl
chr10:123434389..123462971hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828583
hg1928583
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624757
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13953790
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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