A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455761



Internal ID233836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13875775..13876874hg38UCSC Ensembl
chr6:13876006..13877105hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455761
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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