A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950819



Internal ID34573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45207540..45208090hg38UCSC Ensembl
chr4:45209557..45210107hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38551
hg19551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950819
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.051843


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