A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894560



Internal ID22669633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:118843886..118848720hg38UCSC Ensembl
chr6:119165049..119169883hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384835
hg194835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421607
Samples
Known GenesMCM9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894560
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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