A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578073



Internal ID21770116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131242686..131243447hg38UCSC Ensembl
chr9:134118073..134118834hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578073
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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