A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503818



Internal ID20877075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3092163..3371457hg38UCSC Ensembl
chr17:2995457..3274751hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38279295
hg19279295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182419
Samples
Known GenesOR1A1, OR1A2, OR1D2, OR1D4, OR1G1, OR3A1, OR3A2, OR3A4P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503818
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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