A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560198



Internal ID21884553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725414..77725414hg38UCSC Ensembl
chr7:77354731..77354731hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074180
Supporting Variants
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560198
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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