A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511313



Internal ID20884640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35570087..35574100hg38UCSC Ensembl
chr17:33897106..33901119hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg384014
hg194014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182667
Samples
Known GenesSNORD7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511313
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