A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993586



Internal ID20560626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68542250..68544519hg38UCSC Ensembl
chr11:68309718..68311987hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382270
hg192270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475314
Supporting Variants
Samples
Known GenesPPP6R3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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