A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509708



Internal ID286356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6532478..6533262hg38UCSC Ensembl
chr12:6641644..6642428hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509708
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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