A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441396



Internal ID22107576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71688351..71688351hg38UCSC Ensembl
chr10:73448108..73448108hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38914
hg19914
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765945
Samples
Known GenesCDH23
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441396
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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