A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028400



Internal ID20595440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98513259..98515870hg38UCSC Ensembl
chr15:99056488..99059099hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382612
hg192612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502542
Supporting Variants
Samples
Known GenesFAM169B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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