A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17468219



Internal ID22526108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9606770..9608189hg38UCSC Ensembl
chr12:9759366..9760785hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852622
Supporting Variants
Samples
Known GenesKLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17468219
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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