A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507870



Internal ID284577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19763014..19763903hg38UCSC Ensembl
chr12:19915948..19916837hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17056219
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507870
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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