A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556789



Internal ID329916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51881905..51886105hg38UCSC Ensembl
chr1:52347577..52351777hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384201
hg194201
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902753
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556789
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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