A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444667



Internal ID22110847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14652438..14652438hg38UCSC Ensembl
chr1:14978934..14978934hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761297
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444667
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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