A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465914



Internal ID21123467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8787801..8795400hg38UCSC Ensembl
chr12:8940397..8947996hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1392n223
Supporting Variantsnssv18005274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465914
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