A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197592



Internal ID20764632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:674756..681098hg38UCSC Ensembl
chr18:674756..681098hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg386343
hg196343
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535187
Supporting Variants
Samples
Known GenesENOSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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