A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852012



Internal ID22626947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97192719..97194018hg38UCSC Ensembl
chr9:99955001..99956300hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514954, nssv17514955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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