A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610914



Internal ID6997830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136399743..136416482hg38UCSC Ensembl
chr6:136720881..136737620hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3816740
hg1916740
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1221e214
Supporting Variantsessv12560843, essv12560844, essv12560842
SamplesHG03995, NA21114, NA20875
Known GenesMAP7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610914
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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