A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901236



Internal ID1637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27918018..27925391hg38UCSC Ensembl
chr1:28244529..28251902hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg387374
hg197374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420613
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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