A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223583



Internal ID20790624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66313195..66357853hg38UCSC Ensembl
chr7:65778182..65822840hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3844659
hg1944659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604611
Supporting Variants
Samples
Known GenesTPST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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