A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5866004



Internal ID22640939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127592074..127597650hg38UCSC Ensembl
chr9:130354353..130359929hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg385577
hg195577
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5866004
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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