A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595596



Internal ID21787639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59554887..59554887hg38UCSC Ensembl
chr11:59322360..59322360hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083378
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595596
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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