A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191412



Internal ID20758452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4594269..4628481hg38UCSC Ensembl
chr9:4594269..4628481hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3834213
hg1934213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420480
Supporting Variants
Samples
Known GenesSPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191412
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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