A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444593



Internal ID22110773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9170235..9170235hg38UCSC Ensembl
chr1:9230294..9230294hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765810
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444593
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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