A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903664



Internal ID3259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32870813..32870930hg38UCSC Ensembl
chr1:33336414..33336531hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427522
Supporting Variants
Samples
Known GenesFNDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903664
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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