A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997141



Internal ID20564181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116435836..116437518hg38UCSC Ensembl
chr12:116873641..116875323hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg381683
hg191683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6482876
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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