A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945137



Internal ID30757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10785788..10785922hg38UCSC Ensembl
chr4:10787412..10787546hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444905
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945137
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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