A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509698



Internal ID22567648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66480084..66481314hg38UCSC Ensembl
chr8:67392319..67393549hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856363
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509698
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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