A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909032



Internal ID6813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9109939..9112173hg38UCSC Ensembl
chr2:9250068..9252302hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5452068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909032
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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