A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463115



Internal ID241029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3924208..3925899hg38UCSC Ensembl
chr6:3924442..3926133hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381692
hg191692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463115
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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