A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18024693



Internal ID20591733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49581376..49585665hg38UCSC Ensembl
chr15:49873573..49877862hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg384290
hg194290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505035
Supporting Variants
Samples
Known GenesFAM227B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18024693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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