A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510002



Internal ID22567952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81762205..81810372hg38UCSC Ensembl
chr8:82674440..82722607hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3848168
hg1948168
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861364
Supporting Variants
Samples
Known GenesSNX16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510002
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