A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17988726



Internal ID20555766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19758592..19762622hg38UCSC Ensembl
chr11:19780138..19784168hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384031
hg194031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450209
Supporting Variants
Samples
Known GenesMIR4694, NAV2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17988726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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