A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17990257



Internal ID20557298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2974977..2978328hg38UCSC Ensembl
chr11:2996207..2999558hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383352
hg193352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437402
Supporting Variants
Samples
Known GenesNAP1L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17990257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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