A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502680



Internal ID279539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31366903..31367487hg38UCSC Ensembl
chr12:31519837..31520421hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17057131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502680
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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