A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956414



Internal ID38248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142543370..142551085hg38UCSC Ensembl
chr4:143464523..143472238hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg387716
hg197716
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561231
Supporting Variants
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956414
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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