A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150508



Internal ID20717548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96812001..96813800hg38UCSC Ensembl
chr6:97259877..97261676hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611600
Supporting Variants
Samples
Known GenesGPR63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150508
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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