A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508478



Internal ID22566428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88293266..88322878hg38UCSC Ensembl
chr6:89002985..89032597hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3829613
hg1929613
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508478
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