A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501937



Internal ID20875176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75429406..75488336hg38UCSC Ensembl
chr16:75463304..75522234hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3858931
hg1958931
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196063
Samples
Known GenesCFDP1, CHST6, TMEM170A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501937
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