A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155098



Internal ID20722138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46072610..46086451hg38UCSC Ensembl
chr7:46112208..46126049hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3813842
hg1913842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612871
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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