A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17514715



Internal ID22572674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88656363..88661849hg38UCSC Ensembl
chr9:91271278..91276764hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385487
hg195487
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17514715
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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