A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471777



Internal ID21129330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10409296..10409915hg38UCSC Ensembl
chr12:10561895..10562514hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995683
Samples
Known GenesKLRC4, KLRC4-KLRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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