A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997129



Internal ID20564169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116253801..116254800hg38UCSC Ensembl
chr12:116691606..116692605hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486822
Supporting Variants
Samples
Known GenesMED13L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00059


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