A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998735



Internal ID20565775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122641136..122652511hg38UCSC Ensembl
chr12:123125683..123137058hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3811376
hg1911376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487921
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998735
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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