A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151846



Internal ID20718886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12216593..12217053hg38UCSC Ensembl
chr7:12256219..12256679hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601771
Supporting Variants
Samples
Known GenesTMEM106B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00076


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