A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508999



Internal ID285670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19519802..19520626hg38UCSC Ensembl
chr11:19541349..19542173hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38825
hg19825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044731
Samples
Known GenesNAV2, NAV2-AS4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508999
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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