A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180467



Internal ID20747507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50256366..50343749hg38UCSC Ensembl
chr11:50215537..50302920hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3887384
hg1987384
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458595
Supporting Variants
Samples
Known GenesLOC441601
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00107


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