A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564053



Internal ID336976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37910359..37910410hg38UCSC Ensembl
chr6:37878135..37878186hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38581
hg19581
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980603
Samples
Known GenesZFAND3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564053
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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