A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567899



Internal ID21759942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43070540..43071123hg38UCSC Ensembl
chr7:43110139..43110722hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38584
hg19584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016549
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567899
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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