A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17979029



Internal ID20546069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13520424..13522157hg38UCSC Ensembl
chr10:13562424..13564157hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381734
hg191734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17979029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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