A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504988



Internal ID20878253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15729601..15775200hg38UCSC Ensembl
chr17:15632915..15678514hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3845600
hg1945600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3008n223
Supporting Variantsnssv18178396
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504988
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