A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505675



Internal ID22563619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:118697029..118755392hg38UCSC Ensembl
chr8:119709268..119767631hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3858364
hg1958364
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855780
Supporting Variants
Samples
Known GenesSAMD12-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505675
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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