A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947372



Internal ID32283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37266992..37267659hg38UCSC Ensembl
chr4:37268614..37269281hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460244
Supporting Variants
Samples
Known GenesKIAA1239
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947372
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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