A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16293146



Internal ID20502364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725424..77725424hg38UCSC Ensembl
chr7:77354741..77354741hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752632
Supporting Variants
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16293146
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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