A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443929



Internal ID22110110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150372763..150372763hg38UCSC Ensembl
chr4:151293915..151293915hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763589
Samples
Known GenesLRBA
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443929
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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