A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611093



Internal ID6998004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143285778..143290166hg38UCSC Ensembl
Innerchr6:143285778..143290166hg38UCSC Ensembl
Outerchr6:143285604..143290344hg38UCSC Ensembl
chr6:143606915..143611303hg19UCSC Ensembl
Innerchr6:143606915..143611303hg19UCSC Ensembl
Outerchr6:143606741..143611481hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384389
hg194389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12574704, essv12574705, essv12574706, essv12574707
SamplesNA20320, NA19923, NA19093, HG02851
Known GenesAIG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611093
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer