A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176752



Internal ID20743793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126662478..126664344hg38UCSC Ensembl
chr9:129424757..129426623hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448847
Supporting Variants
Samples
Known GenesLMX1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176752
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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