A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177834



Internal ID20744874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35949129..35961212hg38UCSC Ensembl
chr17:34276133..34288216hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3812084
hg1912084
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6497710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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