A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439363



Internal ID22105540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3776773..3776773hg38UCSC Ensembl
chr6:3777007..3777007hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767079
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439363
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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