A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438988



Internal ID22105165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1533765..1533765hg38UCSC Ensembl
chr6:1534000..1534000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762197
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438988
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer