A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175538



Internal ID20742578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19124948..19128218hg38UCSC Ensembl
chr9:19124946..19128216hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg383271
hg193271
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425510
Supporting Variants
Samples
Known GenesPLIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175538
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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