A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610863



Internal ID6997780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133708765..133714418hg38UCSC Ensembl
chr6:134029903..134035556hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385654
hg195654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220e214
Supporting Variantsessv12557518, essv12557515, essv12557516, essv12557517
SamplesHG01842, HG01858, HG02371, HG02396
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610863
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