A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628442



Internal ID7015266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7783696..7793896hg38UCSC Ensembl
chr12:7936292..7946492hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3810201
hg1910201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14349725
SamplesNA11918
Known GenesNANOG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628442
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