A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510296



Internal ID22568246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96716785..96719214hg38UCSC Ensembl
chr8:97729013..97731442hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382430
hg192430
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859815
Supporting Variants
Samples
Known GenesCPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510296
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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