A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465200



Internal ID21122753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52936644..52941594hg38UCSC Ensembl
chr12:53330428..53335378hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg384951
hg194951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001415
Samples
Known GenesKRT8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465200
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