A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946464



Internal ID31669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:29904072..29905352hg38UCSC Ensembl
chr4:29905694..29906974hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg381281
hg191281
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946464
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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