A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218915



Internal ID20785955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87112901..87167700hg38UCSC Ensembl
chr6:87822619..87877418hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3854800
hg1954800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409455
Supporting Variants
Samples
Known GenesZNF292
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218915
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00076


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