A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217702



Internal ID20784742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104942469..104960246hg38UCSC Ensembl
chr7:104582916..104600693hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3817778
hg1917778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217702
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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