A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608308



Internal ID6995238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21361504..21366954hg38UCSC Ensembl
Innerchr6:21361504..21366954hg38UCSC Ensembl
Outerchr6:21361431..21367032hg38UCSC Ensembl
chr6:21361735..21367185hg19UCSC Ensembl
Innerchr6:21361735..21367185hg19UCSC Ensembl
Outerchr6:21361662..21367263hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12220184, essv12220181, essv12220178, essv12220183, essv12220179, essv12220182, essv12220177, essv12220180
SamplesNA19066, NA18988, NA19068, NA18986, NA18516, NA18610, NA19474, NA19463
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608308
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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