A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998534



Internal ID20565574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28933301..28933795hg38UCSC Ensembl
chr12:29086234..29086728hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461271
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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