A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513428



Internal ID22571383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42473706..42495579hg38UCSC Ensembl
chr9:44475540..44497413hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3821874
hg1921874
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513428
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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