A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959072



Internal ID40024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163921991..163935295hg38UCSC Ensembl
chr4:164843143..164856447hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3813305
hg1913305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454086
Supporting Variants
Samples
Known GenesMARCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959072
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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