A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610727



Internal ID6650953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127723211..127729005hg38UCSC Ensembl
chr6:128044356..128050150hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg385795
hg195795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1218e214
Supporting Variantsessv12541109
SamplesHG03419
Known GenesTHEMIS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610727
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