A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449158



Internal ID22115335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26163321..26163647hg38UCSC Ensembl
chr1:26489812..26490138hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766263
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449158
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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