A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607873



Internal ID6994804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:861301..887630hg38UCSC Ensembl
chr6:861301..887630hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3826330
hg1926330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12172012
SamplesHG03711
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607873
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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