A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903606



Internal ID3223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32268222..32269786hg38UCSC Ensembl
chr1:32733823..32735387hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420680
Supporting Variants
Samples
Known GenesLCK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903606
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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