A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165837



Internal ID20732877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:3030965..3031167hg38UCSC Ensembl
chr8:2888487..2888689hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426554
Supporting Variants
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00119


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