A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992651



Internal ID20559691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60582384..60583068hg38UCSC Ensembl
chr11:60349857..60350541hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473721
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992651
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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