A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18047929



Internal ID20614969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40195782..40197523hg38UCSC Ensembl
chr19:40701689..40703430hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg381742
hg191742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524387
Supporting Variants
Samples
Known GenesMAP3K10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18047929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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