A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902780



Internal ID22677941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149786061..149786389hg38UCSC Ensembl
chr6:150107197..150107525hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416971
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902780
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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