A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610222



Internal ID6997139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103556302..103591801hg38UCSC Ensembl
chr6:104004177..104039676hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3835500
hg1935500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12490794, essv12490795
SamplesHG01119, HG01464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610222
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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