A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570741



Internal ID21762784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:410977..411066hg38UCSC Ensembl
chr7:450943..451032hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570741
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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