A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513938



Internal ID22571896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64034872..64046105hg38UCSC Ensembl
chrUn_gl000211:66425..77658hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3811234
hg1911234
Variant TypeOTHER copy number variation
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513938
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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