A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236896



Internal ID20803936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97151035..97155477hg38UCSC Ensembl
chr7:96780347..96784789hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614030
Supporting Variants
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236896
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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