A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610242



Internal ID6997159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104416510..104488616hg38UCSC Ensembl
chr6:104864385..104936491hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3872107
hg1972107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12495643, essv12495641, essv12495640, essv12495642, essv12495644
SamplesHG00143, HG03821, HG03667, NA19190, HG03919
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610242
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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