A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452048



Internal ID22509920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21484601..21489169hg38UCSC Ensembl
chr10:21773530..21778098hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg384569
hg194569
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857219
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452048
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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