A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524265



Internal ID20897626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3336264..3349891hg38UCSC Ensembl
chr18:3336262..3349889hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3813628
hg1913628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184595
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524265
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