A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513941



Internal ID22571899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64040254..64060816hg38UCSC Ensembl
chrUn_gl000211:71807..92369hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3820563
hg1920563
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863863
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513941
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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