A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16889209



Internal ID166899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150995013..150996274hg38UCSC Ensembl
chr1:150967489..150968750hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg381262
hg191262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416769
Supporting Variants
Samples
Known GenesANXA9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16889209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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