A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052988



Internal ID103172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1508880..1508880hg38UCSC Ensembl
chr12:1618046..1618046hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052988
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.113019


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