A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230197



Internal ID20797237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145068701..145093300hg38UCSC Ensembl
chr7:144765794..144790393hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3824600
hg1924600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415734
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230197
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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