A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909010



Internal ID6798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5696117..5696317hg38UCSC Ensembl
chr2:5836249..5836449hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446558
Supporting Variants
Samples
Known GenesSOX11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909010
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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