A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231919



Internal ID20798959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51976060..52509645hg38UCSC Ensembl
chr7:52043756..52577341hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38533586
hg19533586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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