A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951154



Internal ID34794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57033157..57033157hg38UCSC Ensembl
chr4:57899323..57899323hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543579
Supporting Variants
Samples
Known GenesIGFBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951154
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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