A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988329



Internal ID20555369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14615587..14616388hg38UCSC Ensembl
chr11:14637133..14637934hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451807
Supporting Variants
Samples
Known GenesPSMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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