A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610568



Internal ID6997485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120661627..120700081hg38UCSC Ensembl
chr6:120982773..121021227hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3838455
hg1938455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1214e214
Supporting Variantsessv12524390, essv12524389, essv12524388
SamplesNA18605, HG00623, NA18957
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610568
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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