A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3630719



Internal ID6670853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109485009..109700854hg38UCSC Ensembl
Innerchr12:109485159..109700704hg38UCSC Ensembl
Outerchr12:109484859..109701004hg38UCSC Ensembl
chr12:109922814..110138659hg19UCSC Ensembl
Innerchr12:109922964..110138509hg19UCSC Ensembl
Outerchr12:109922664..110138809hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38215846
hg19215846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14603927, essv14603925, essv14603922, essv14603926, essv14603923, essv14603924
SamplesHG01702, NA20759, HG02322, HG00623, HG01357, HG01137
Known GenesMMAB, MVK, UBE3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3630719
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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