A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509692



Internal ID22567642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65933230..65936929hg38UCSC Ensembl
chr8:66845465..66849164hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5858036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509692
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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