A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735674



Internal ID159340
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 StatusS
Merged Variantsnsv5554349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735674
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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