A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026987



Internal ID20594027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88103261..88106804hg38UCSC Ensembl
chr15:88646492..88650035hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg383544
hg193544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503122
Supporting Variants
Samples
Known GenesNTRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026987
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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