A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999614



Internal ID20566654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18851989..18853354hg38UCSC Ensembl
chr12:19004923..19006288hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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