A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948561



Internal ID33078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24339364..24342174hg38UCSC Ensembl
chr4:24340987..24343797hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382811
hg192811
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555799
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948561
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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