A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954096



Internal ID36727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118766354..118766422hg38UCSC Ensembl
chr4:119687509..119687577hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472348
Supporting Variants
Samples
Known GenesSEC24D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954096
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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