A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574811



Internal ID21766854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7953218..7953218hg38UCSC Ensembl
chr7:7992849..7992849hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072923
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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