A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563604



Internal ID336536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229177883..229177897hg38UCSC Ensembl
chr1:229313630..229313644hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3815
hg1915
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16898301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563604
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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