A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473793



Internal ID251475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37712970..37917713hg38UCSC Ensembl
chr6:37680746..37885489hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38204744
hg19204744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980586
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473793
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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