A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044957



Internal ID20611997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10962955..10968075hg38UCSC Ensembl
chr19:11073631..11078751hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg385121
hg195121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527274
Supporting Variants
Samples
Known GenesSMARCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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