A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992356



Internal ID20559396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4976201..5005600hg38UCSC Ensembl
chr11:4997431..5026830hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3829400
hg1929400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444564
Supporting Variants
Samples
Known GenesMMP26, OR51L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992356
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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