A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13963413



Internal ID4983787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124932102..124937760hg38UCSC Ensembl
chr10:126620671..126626329hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg385659
hg195659
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624822
Supporting Variants
SamplesNA18486
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13963413
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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