A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465621



Internal ID21123174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12879339..12905014hg38UCSC Ensembl
chr12:13032273..13057948hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3825676
hg1925676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1424n223
Supporting Variantsnssv17997566
Samples
Known GenesGPRC5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465621
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