A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236357



Internal ID20803397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79156108..79181291hg38UCSC Ensembl
chr7:78785424..78810607hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3825184
hg1925184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610247
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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