A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509041



Internal ID22566991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98652228..98661924hg38UCSC Ensembl
chr6:99100104..99109800hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg389697
hg199697
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509041
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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