A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852731



Internal ID22627666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5653147..5654446hg38UCSC Ensembl
chr9:5653147..5654446hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2057n209
Supporting Variantsnssv17513722, nssv17513721
Samples
Known GenesKIAA1432
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852731
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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