A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514524



Internal ID22572482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85531539..85538423hg38UCSC Ensembl
chr9:88146454..88153338hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg386885
hg196885
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514524
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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