A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527805



Internal ID20901166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3066424..3100086hg38UCSC Ensembl
chr20:3047070..3080732hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833663
hg1933663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202609
Samples
Known GenesAVP, OXT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527805
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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