A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889886



Internal ID22664908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89810331..89816294hg38UCSC Ensembl
chr6:90520050..90526013hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385964
hg195964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446487
Samples
Known GenesMDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889886
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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