A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219246



Internal ID20786286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142451680..142470384hg38UCSC Ensembl
chr7:142161560..142180283hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3818705
hg1918724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423321
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219246
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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