A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595684



Internal ID6635958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28220995..28252565hg38UCSC Ensembl
Innerchr3:28220995..28252565hg38UCSC Ensembl
Outerchr3:28220495..28253065hg38UCSC Ensembl
chr3:28262486..28294056hg19UCSC Ensembl
Innerchr3:28262486..28294056hg19UCSC Ensembl
Outerchr3:28261986..28294556hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3831571
hg1931571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10961936
SamplesNA19792
Known GenesCMC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595684
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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