A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505931



Internal ID22563876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29702994..29706143hg38UCSC Ensembl
chr8:29560510..29563659hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383150
hg193150
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858400
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505931
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