A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904111



Internal ID3560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61112815..61112815hg38UCSC Ensembl
chr1:61578487..61578487hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547186
Supporting Variants
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904111
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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