A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442376



Internal ID22108559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12513433..12513433hg38UCSC Ensembl
chrY:14625233..14625233hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760002
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442376
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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