A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980971



Internal ID54689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11414852..11423572hg38UCSC Ensembl
chr6:11415085..11423805hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg388721
hg198721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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