A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182527



Internal ID20749567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132118347..132282945hg38UCSC Ensembl
chr10:133931851..134096449hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38164599
hg19164599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448781
Supporting Variants
Samples
Known GenesDPYSL4, JAKMIP3, STK32C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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