A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175532



Internal ID20742572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19103510..19138635hg38UCSC Ensembl
chr9:19103508..19138633hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3835126
hg1935126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422335
Supporting Variants
Samples
Known GenesPLIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175532
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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