A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4448892



Internal ID22115070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15209301..15209301hg38UCSC Ensembl
chr10:15251300..15251300hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383774
hg193774
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765085
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4448892
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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