A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445072



Internal ID22111252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156735501..156735501hg38UCSC Ensembl
chr1:156705293..156705293hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768527
Samples
Known GenesRRNAD1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445072
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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