A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456918



Internal ID234975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10419220..10419372hg38UCSC Ensembl
chr6:10419453..10419605hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979557
Samples
Known GenesTFAP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456918
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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