A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18027999



Internal ID20595039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99705325..99705878hg38UCSC Ensembl
chr15:100245530..100246083hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496812
Supporting Variants
Samples
Known GenesMEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18027999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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