A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443953



Internal ID22110134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99900292..99900292hg38UCSC Ensembl
chr10:101660049..101660049hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765103
Samples
Known GenesDNMBP
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443953
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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