A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562699



Internal ID335644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52838442..52839204hg38UCSC Ensembl
chr4:53704609..53705371hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16951000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562699
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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