A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610326



Internal ID6997243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108757175..108762009hg38UCSC Ensembl
Innerchr6:108757175..108762009hg38UCSC Ensembl
Outerchr6:108757016..108762206hg38UCSC Ensembl
chr6:109078378..109083212hg19UCSC Ensembl
Innerchr6:109078378..109083212hg19UCSC Ensembl
Outerchr6:109078219..109083409hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384835
hg194835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499701, essv12499699, essv12499702, essv12499700, essv12499703
SamplesHG01885, NA20356, NA19385, NA19159, NA19213
Known GenesLINC00222
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610326
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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