A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876007



Internal ID22650967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10944360..10953179hg38UCSC Ensembl
chrUn_gl000241:19788..28607hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388820
hg198820
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488992, nssv17488991
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876007
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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