A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506774



Internal ID22564722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47667106..47669794hg38UCSC Ensembl
chr8:48579668..48582356hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg382689
hg192689
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859223
Supporting Variants
Samples
Known GenesSPIDR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506774
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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