A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864646



Internal ID22639581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110633400..110638747hg38UCSC Ensembl
chr9:113395680..113401027hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385348
hg195348
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510773
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864646
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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