A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444592



Internal ID22110772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9129265..9129265hg38UCSC Ensembl
chr1:9189324..9189324hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759111
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444592
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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