A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16951156



Internal ID34795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57084035..57084053hg38UCSC Ensembl
chr4:57950201..57950219hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546191
Supporting Variants
Samples
Known GenesIGFBP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16951156
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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