A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579758



Internal ID21771801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36474249..36475082hg38UCSC Ensembl
chr9:36474246..36475079hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020257
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579758
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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