A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3594888



Internal ID6635163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:210087..263700hg38UCSC Ensembl
chr3:251770..305383hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3853614
hg1953614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv853e214
Supporting Variantsessv10897458, essv10897459
SamplesHG02769, HG02238
Known GenesCHL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3594888
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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