A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925305



Internal ID22700532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89339290..89539687hg38UCSC Ensembl
chr11:89072458..89272855hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38200398
hg19200398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358496
Samples
Known GenesNOX4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925305
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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