A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558479



Internal ID21882834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32531415..32531415hg38UCSC Ensembl
chr7:32571027..32571027hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076063
Supporting Variants
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558479
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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