A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527220



Internal ID20900581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4320080..4388602hg38UCSC Ensembl
chr19:4320077..4388599hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3868523
hg1968523
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198567
Samples
Known GenesFSD1, MPND, SH3GL1, STAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527220
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