A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470384



Internal ID21127937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:23514388..23522360hg38UCSC Ensembl
chr12:23667322..23675294hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg387973
hg197973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470384
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