A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12554763



Internal ID2556579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132756695..132762169hg38UCSC Ensembl
chr6:133077834..133083308hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385475
hg195475
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3610845
Supporting Variants
SamplesHG03786
Known GenesVNN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12554763
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