A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465627



Internal ID21123180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:51051668..51052742hg38UCSC Ensembl
chr12:51445451..51446525hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg381075
hg191075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18001300
Samples
Known GenesLETMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465627
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