A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444604



Internal ID22110784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101304496..101304496hg38UCSC Ensembl
chr1:101770052..101770052hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759686
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444604
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer