A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603444



Internal ID6643698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183655300..183661232hg38UCSC Ensembl
chr4:184576453..184582385hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg385933
hg195933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11732427
SamplesHG01619
Known GenesRWDD4, TRAPPC11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603444
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