A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559164



Internal ID21883519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23187909..23187960hg38UCSC Ensembl
chr7:23227528..23227579hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6008837
Supporting Variants
Samples
Known GenesNUPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559164
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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