A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509708



Internal ID22567658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66937774..66942120hg38UCSC Ensembl
chr8:67850009..67854355hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg384347
hg194347
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854735
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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