A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900382



Internal ID1042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25767167..25767379hg38UCSC Ensembl
chr1:26093658..26093870hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417375
Supporting Variants
Samples
Known GenesMAN1C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900382
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.061037


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