A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446751



Internal ID22112929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21158293..21158293hg38UCSC Ensembl
chr2:21381165..21381165hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757072
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446751
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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