A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616584



Internal ID21808631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9001675..9010780hg38UCSC Ensembl
chr12:9154271..9163376hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg389106
hg199106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6030945
Supporting Variants
Samples
Known GenesKLRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616584
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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