A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506761



Internal ID22564709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47299692..47302781hg38UCSC Ensembl
chr8_gl000196_random:4141..6510hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383090
hg192370
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859913
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506761
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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