A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998962



Internal ID20566002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30871582..30875329hg38UCSC Ensembl
chr12:31024516..31028263hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg383748
hg193748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998962
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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