A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951145



Internal ID34787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56944579..56949602hg38UCSC Ensembl
chr4:57810745..57815768hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg385024
hg195024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951145
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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