A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145689



Internal ID20712729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65101408..65354690hg38UCSC Ensembl
chr6:65811301..66064583hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38253283
hg19253283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409396
Supporting Variants
Samples
Known GenesEYS, LOC441155
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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