A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609412



Internal ID6996333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69492727..69513108hg38UCSC Ensembl
chr6:70202619..70223000hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3820382
hg1920382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12410125, essv12410126, essv12410124
SamplesHG01527, HG02571, HG02570
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609412
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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