A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961251



Internal ID41474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182970432..182970531hg38UCSC Ensembl
chr4:183891585..183891684hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563121
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961251
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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