A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437777



Internal ID22103957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214869191..214869191hg38UCSC Ensembl
chr1:215042534..215042534hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760221
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437777
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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