A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192063



Internal ID20759103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:1087496..1201121hg38UCSC Ensembl
chr18:1087497..1201122hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38113626
hg19113626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer