A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903112



Internal ID2894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60232015..60600809hg38UCSC Ensembl
chr1:60697687..61066481hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38368795
hg19368795
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430660
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903112
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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