A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564456



Internal ID21888811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43308291..43308291hg38UCSC Ensembl
chr7:43347890..43347890hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6078840
Supporting Variants
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564456
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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