A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445005



Internal ID22111185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155954238..155954238hg38UCSC Ensembl
chr1:155924029..155924029hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762235
Samples
Known GenesARHGEF2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445005
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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