A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18042734



Internal ID20609774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70294462..70297010hg38UCSC Ensembl
chr18:67961698..67964246hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg382549
hg192549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6517063
Supporting Variants
Samples
Known GenesSOCS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18042734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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