A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561057



Internal ID334045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27795904..27801296hg38UCSC Ensembl
chr1:28122415..28127807hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg385393
hg195393
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901214
Samples
Known GenesSTX12
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561057
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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