A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17467846



Internal ID22525736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45390201..45396417hg38UCSC Ensembl
chr10:45885649..45891865hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg386217
hg196217
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863687
Supporting Variants
Samples
Known GenesALOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17467846
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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