A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862077



Internal ID22637012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65525740..65537625hg38UCSC Ensembl
chr9:44802476..44814216hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811886
hg1911741
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514027, nssv17514026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862077
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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