A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512577



Internal ID20885912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75579400..75580542hg38UCSC Ensembl
chr16:75613298..75614440hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381143
hg191143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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