A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510097



Internal ID22568047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85280856..85296148hg38UCSC Ensembl
chr8:86193085..86208377hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3815293
hg1915293
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856378
Supporting Variants
Samples
Known GenesCA13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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