A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149706



Internal ID20716746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88090501..88092900hg38UCSC Ensembl
chr6:88800219..88802618hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403571
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149706
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00116


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