A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514219



Internal ID22572177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71953409..71958108hg38UCSC Ensembl
chr9:74568325..74573024hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849344
Supporting Variants
Samples
Known GenesC9orf85
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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