A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17508489



Internal ID22566439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89132282..89137215hg38UCSC Ensembl
chr6:89842001..89846934hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384934
hg194934
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845750
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17508489
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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