A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595502



Internal ID6982820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21211496..21297735hg38UCSC Ensembl
chr3:21252988..21339227hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3886240
hg1986240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv875e214
Supporting Variantsessv10946973, essv10946974, essv10946975
SamplesHG01311, NA20534, NA11881
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595502
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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