A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531692



Internal ID20905053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1595601..1749500hg38UCSC Ensembl
chr18:1595602..1749501hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38153900
hg19153900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3263n223
Supporting Variantsnssv18195000
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531692
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