A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609005



Internal ID6649238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52762755..52797076hg38UCSC Ensembl
chr6:52627553..52661874hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3834322
hg1934322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12351690, essv12351693, essv12351691, essv12351692
SamplesNA20805, NA18960, NA20507, HG01164
Known GenesGSTA1, GSTA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609005
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