A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186185



Internal ID20753225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:83570601..83631200hg38UCSC Ensembl
chr13:84144736..84205335hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3860600
hg1960600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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