A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439413



Internal ID22105591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36429013..36429013hg38UCSC Ensembl
chr6:36396790..36396790hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766040
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439413
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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