A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506777



Internal ID22564725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47763663..47764925hg38UCSC Ensembl
chr8:48676224..48677486hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg381263
hg191263
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863045
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506777
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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