A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922663



Internal ID22697888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166372399..166372458hg38UCSC Ensembl
chr6:166785887..166785946hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415544
Samples
Known GenesMPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922663
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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