A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13927747



Internal ID6168827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106334285..106420194hg38UCSC Ensembl
chr10:108094043..108179952hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3885910
hg1985910
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624470
Supporting Variants
SamplesNA19707
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13927747
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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