A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17511554



Internal ID22569506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130640002..130644053hg38UCSC Ensembl
chr9:133515389..133519440hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg384052
hg194052
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850335
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17511554
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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