A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595775



Internal ID6636049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32401608..32404289hg38UCSC Ensembl
Innerchr3:32401608..32404289hg38UCSC Ensembl
Outerchr3:32401316..32404555hg38UCSC Ensembl
chr3:32443100..32445781hg19UCSC Ensembl
Innerchr3:32443100..32445781hg19UCSC Ensembl
Outerchr3:32442808..32446047hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg382682
hg192682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10975140, essv10975142, essv10975141
SamplesNA19443, HG02088, NA18965
Known GenesCMTM7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595775
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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