A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221256



Internal ID20788296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74434992..74444761hg38UCSC Ensembl
chr7:73849322..73859091hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg389770
hg199770
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617118
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221256
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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