A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501610



Internal ID20874846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81510482..81514507hg38UCSC Ensembl
chr16:81544087..81548112hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384026
hg194026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032888
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501610
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