A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644885



Internal ID7031636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57006900..57082584hg38UCSC Ensembl
chr19:57518268..57593952hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3875685
hg1975685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16106502
SamplesNA19019
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644885
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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