A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759049



Internal ID20534909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149786178..149786178hg38UCSC Ensembl
chr6:150107314..150107314hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290444
Samples
Known GenesPCMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759049
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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