A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509150



Internal ID22567100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33211444..33216684hg38UCSC Ensembl
chr8:33068962..33074202hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385241
hg195241
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854050
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509150
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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