A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508973



Internal ID20882278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:12219496..12266072hg38UCSC Ensembl
chr17:12122813..12169389hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3846577
hg1946577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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