A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17513417



Internal ID22571372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42457534..42465916hg38UCSC Ensembl
chr9:44505203..44513585hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388383
hg198383
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5849222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17513417
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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