A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437826



Internal ID22104007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217524940..217524940hg38UCSC Ensembl
chr1:217698282..217698282hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765952
Samples
Known GenesGPATCH2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437826
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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