A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228854



Internal ID20795894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87002101..87014900hg38UCSC Ensembl
chr6:87711819..87724618hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411994
Supporting Variants
Samples
Known GenesHTR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228854
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00031


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