A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151874



Internal ID20718914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12240381..12240944hg38UCSC Ensembl
chr7:12280007..12280570hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00034


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