A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437624



Internal ID22103804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56075632..56075632hg38UCSC Ensembl
chr12:56469416..56469416hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761383
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437624
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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