A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505981



Internal ID22563926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34945441..34965684hg38UCSC Ensembl
chr8:34802959..34823202hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3820244
hg1920244
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505981
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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