A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509879



Internal ID22567829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74543392..74550241hg38UCSC Ensembl
chr8:75455627..75462476hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg386850
hg196850
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860754
Supporting Variants
Samples
Known GenesMIR5681A, MIR5681B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509879
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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