A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605230



Internal ID20978301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158997850..158998272hg38UCSC Ensembl
chr6:159418882..159419304hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18142019
Samples
Known GenesRSPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605230
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