A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858000



Internal ID22632935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131265581..131274981hg38UCSC Ensembl
chr7:130950340..130959740hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg389401
hg199401
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17503937
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858000
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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