A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554349



Internal ID327539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50570361..50570641hg38UCSC Ensembl
chr7:50638058..50638338hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554349
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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