A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999999



Internal ID20567039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21010341..21011905hg38UCSC Ensembl
chr12:21163275..21164839hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473481
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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