A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17999066



Internal ID20566106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40194201..40198400hg38UCSC Ensembl
chr12:40588003..40592202hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17999066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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