A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754998



Internal ID20530858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71750186..71750186hg38UCSC Ensembl
chr9:74365102..74365102hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290877
Samples
Known GenesTMEM2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754998
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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