A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957214



Internal ID38784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155187626..155188291hg38UCSC Ensembl
chr4:156108778..156109443hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38666
hg19666
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957214
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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