A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005834



Internal ID20572874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9476301..9600100hg38UCSC Ensembl
chr12:9628897..9752696hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38123800
hg19123800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461174
Supporting Variants
Samples
Known GenesKLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.54607


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