A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316611



Internal ID20849691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158546769..158575460hg38UCSC Ensembl
chr1:158516559..158545250hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3828692
hg1928692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200952
Samples
Known GenesOR6P1, OR6Y1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316611
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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