A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643681



Internal ID6683752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11894499..11919495hg38UCSC Ensembl
chr19:12005314..12030310hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3824997
hg1924997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv653e214
Supporting Variantsessv15991071
SamplesNA20785
Known GenesZNF69
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643681
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