A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439742



Internal ID22105919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40079153..40079153hg38UCSC Ensembl
chr6:40046892..40046892hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764256
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439742
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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