A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517063



Internal ID20890424
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 StatusM
Merged Variants
Supporting Variantsnssv18042734
Samples
Known GenesSOCS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517063
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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