A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231326



Internal ID20798366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1378066..1409579hg38UCSC Ensembl
chr7:1417702..1449215hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3831514
hg1931514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600226
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231326
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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