A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508120



Internal ID20881418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88620291..88621262hg38UCSC Ensembl
chr16:88686699..88687670hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033213
Samples
Known GenesZC3H18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508120
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