A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527788



Internal ID303873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27849643..27854510hg38UCSC Ensembl
chr16:27860964..27865831hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384868
hg194868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706292
Samples
Known GenesGSG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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