A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841147



Internal ID22616082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138403806..138408109hg38UCSC Ensembl
chr5:137739495..137743798hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg384304
hg194304
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495555, nssv17495554
Samples
Known GenesKDM3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841147
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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