A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579888



Internal ID21771931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72502674..72502752hg38UCSC Ensembl
chr11:72213718..72213796hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035500
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579888
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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