A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443528



Internal ID22109711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101334376..101334376hg38UCSC Ensembl
chr13:101986727..101986727hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767857
Samples
Known GenesNALCN
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443528
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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