A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059031



Internal ID107226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60997599..61031576hg38UCSC Ensembl
chr12:61391380..61425357hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3833978
hg1933978
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17059031
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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