A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503379



Internal ID20876634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57106611..57106699hg38UCSC Ensembl
chr16:57140523..57140611hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029772
Samples
Known GenesCPNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503379
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