A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452952



Internal ID22510825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45510424..45513218hg38UCSC Ensembl
chr10:46005872..46008666hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382795
hg192795
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857080
Supporting Variants
Samples
Known GenesMARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452952
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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