A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957608



Internal ID39046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148196330..148199536hg38UCSC Ensembl
chr4:149117481..149120687hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg383207
hg193207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459656
Supporting Variants
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957608
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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