A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228311



Internal ID20795351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78536363..78544950hg38UCSC Ensembl
chr7:78165680..78174267hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg388588
hg198588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602723
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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