A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150479



Internal ID20717519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96538901..96540000hg38UCSC Ensembl
chr6:96986777..96987876hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610120
Supporting Variants
Samples
Known GenesUFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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