A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947167



Internal ID32139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35821102..35840224hg38UCSC Ensembl
chr4:35822724..35841846hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3819123
hg1919123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947167
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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