A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149809



Internal ID20716849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95604701..95605300hg38UCSC Ensembl
chr6:96052577..96053176hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409255
Supporting Variants
Samples
Known GenesMANEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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