A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439786



Internal ID22105963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43958628..43958628hg38UCSC Ensembl
chr6:43926365..43926365hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758310
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439786
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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