A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444500



Internal ID22110680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120775374..120775374hg38UCSC Ensembl
chr10:122534886..122534886hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761610
Samples
Known GenesMIR5694, WDR11-AS1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444500
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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