A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225740



Internal ID20792780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13849448..13862600hg38UCSC Ensembl
chr7:13889073..13902225hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3813153
hg1913153
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225740
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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