A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484688



Internal ID21142241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122097197..122101606hg38UCSC Ensembl
chr12:122581744..122586153hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997835
Samples
Known GenesMLXIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484688
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