A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040632



Internal ID94796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3796972..3797033hg38UCSC Ensembl
chr11:3818202..3818263hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497290
Supporting Variants
Samples
Known GenesNUP98
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040632
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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