A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512304



Internal ID288861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6319842..6319969hg38UCSC Ensembl
chr12:6429008..6429135hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054653
Samples
Known GenesPLEKHG6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512304
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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