A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183769



Internal ID20750809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17667662..17673015hg38UCSC Ensembl
chr10:17709661..17715014hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg385354
hg195354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441655
Supporting Variants
Samples
Known GenesSTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183769
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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