A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150483



Internal ID20717523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96563701..96564400hg38UCSC Ensembl
chr6:97011577..97012276hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607314
Supporting Variants
Samples
Known GenesFHL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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