A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509221



Internal ID22567171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43080904..43084003hg38UCSC Ensembl
chr8:42936047..42939146hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861338
Supporting Variants
Samples
Known GenesFNTA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509221
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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