A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857531



Internal ID22632466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42472593..42477499hg38UCSC Ensembl
chr9:44493620..44498526hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg384907
hg194907
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17513422, nssv17513423, nssv17513424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857531
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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