A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16953371



Internal ID36267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101869975..101962255hg38UCSC Ensembl
chr4:102791132..102883412hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3892281
hg1992281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466291
Supporting Variants
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16953371
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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