A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229632



Internal ID20796672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145359101..145364800hg38UCSC Ensembl
chr7:145056194..145061893hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416631
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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