A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611098



Internal ID6998009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143562833..143564328hg38UCSC Ensembl
Innerchr6:143562856..143564305hg38UCSC Ensembl
Outerchr6:143562810..143564351hg38UCSC Ensembl
chr6:143883970..143885465hg19UCSC Ensembl
Innerchr6:143883993..143885442hg19UCSC Ensembl
Outerchr6:143883947..143885488hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12574742, essv12574741, essv12574743
SamplesHG03074, HG03697, NA19072
Known GenesLOC285740
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611098
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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