A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470941



Internal ID248686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14685972..14686323hg38UCSC Ensembl
chr6:14686203..14686554hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470941
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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