A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857077



Internal ID22632012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130276776..130291083hg38UCSC Ensembl
chr9:133039055..133053362hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814308
hg1914308
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2204n209
Supporting Variantsnssv17511534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857077
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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