A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569904



Internal ID21761947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:847264..847820hg38UCSC Ensembl
chr7:886901..887457hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015622
Supporting Variants
Samples
Known GenesSUN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569904
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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