A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509722



Internal ID22567672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67634010..67641395hg38UCSC Ensembl
chr8:68546245..68553630hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg387386
hg197386
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854282
Supporting Variants
Samples
Known GenesCPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509722
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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