A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903054



Internal ID2852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56866757..56867077hg38UCSC Ensembl
chr1:57332430..57332750hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431350
Supporting Variants
Samples
Known GenesC8A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903054
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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