A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231583



Internal ID20798624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44745966..44746541hg38UCSC Ensembl
chr7:44785565..44786140hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6612445
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01796


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