A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611105



Internal ID6998016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144224080..144235172hg38UCSC Ensembl
Innerchr6:144224230..144235022hg38UCSC Ensembl
Outerchr6:144223930..144235322hg38UCSC Ensembl
chr6:144545217..144556308hg19UCSC Ensembl
Innerchr6:144545367..144556158hg19UCSC Ensembl
Outerchr6:144545067..144556458hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3811093
hg1911092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12576154
SamplesHG02025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611105
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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