A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439119



Internal ID22105296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71752459..71752459hg38UCSC Ensembl
chr9:74367375..74367375hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762260
Samples
Known GenesTMEM2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439119
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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