A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218141



Internal ID20785181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35966801..35977600hg38UCSC Ensembl
chr7:36006411..36017210hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604825
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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