A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180866



Internal ID20747906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55239494..56220083hg38UCSC Ensembl
chr10:56999254..57979844hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38980590
hg19980591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446248
Supporting Variants
Samples
Known GenesMTRNR2L5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180866
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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