A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271180



Internal ID20480398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10312799..10312877hg38UCSC Ensembl
chr12:10465398..10465476hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740422
Supporting Variants
Samples
Known GenesKLRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271180
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer