A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555962



Internal ID329111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29446712..29449840hg38UCSC Ensembl
chr1:29773224..29776352hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383129
hg193129
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900519
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555962
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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