A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950697



Internal ID34490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71742703..71744253hg38UCSC Ensembl
chr4:72608420..72609970hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381551
hg191551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455029
Supporting Variants
Samples
Known GenesGC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950697
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001562


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