A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451693



Internal ID22509565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45391861..45419343hg38UCSC Ensembl
chr10:45887309..45914791hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3827483
hg1927483
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856637
Supporting Variants
Samples
Known GenesALOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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