A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498095



Internal ID20871303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10842035..10853610hg38UCSC Ensembl
chr17:10745352..10756927hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3811576
hg1911576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498095
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