A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509694



Internal ID22567644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66208504..66209503hg38UCSC Ensembl
chr8:67120739..67121738hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859060
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509694
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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