A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902961



Internal ID2792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:50889526..50908036hg38UCSC Ensembl
chr1:51355198..51373708hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3818511
hg1918511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138125
Supporting Variants
Samples
Known GenesFAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902961
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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