A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088995



Internal ID21491507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88831342..88831665hg38UCSC Ensembl
chr16:88897750..88898073hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589159
Supporting Variants
SamplesNA19238
Known GenesGALNS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088995
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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