A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18000704



Internal ID20567744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31814487..31824778hg38UCSC Ensembl
chr12:31967421..31977712hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3810292
hg1910292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475537
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18000704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer