A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514965



Internal ID22572924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:975611..976662hg38UCSC Ensembl
chr9:975611..976662hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381052
hg191052
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852249
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514965
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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