A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971205



Internal ID48150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143285794..143290130hg38UCSC Ensembl
chr6:143606931..143611267hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384337
hg194337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467740
Supporting Variants
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971205
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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