A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444629



Internal ID22110809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127502445..127502445hg38UCSC Ensembl
chr10:129300709..129300709hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757604
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444629
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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