A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005828



Internal ID20572868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94616375..94618984hg38UCSC Ensembl
chr12:95010151..95012760hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382610
hg192610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467869
Supporting Variants
Samples
Known GenesTMCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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