A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176614



Internal ID20743655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124623647..124628595hg38UCSC Ensembl
chr9:127385926..127390874hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384949
hg194949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450510
Supporting Variants
Samples
Known GenesNR6A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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