A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979557



Internal ID53751
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 StatusS
Merged Variantsnsv5456918
Supporting Variants
Samples
Known GenesTFAP2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979557
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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