A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903448



Internal ID3107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59104462..59109201hg38UCSC Ensembl
chr1:59570134..59574873hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg384740
hg194740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418804
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903448
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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