A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462833



Internal ID21120386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92762126..92762872hg38UCSC Ensembl
chr12:93155902..93156648hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005785
Samples
Known GenesPLEKHG7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462833
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