A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996204



Internal ID20563244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10836555..10837035hg38UCSC Ensembl
chr12:10989154..10989634hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470972
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00067


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