A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231244



Internal ID20798284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97347061..97348004hg38UCSC Ensembl
chr7:96976373..96977316hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38944
hg19944
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231244
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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