A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440521



Internal ID22106699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158353102..158363140hg38UCSC Ensembl
chr4:159274254..159284292hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3810039
hg1910039
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763123
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SUBSDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440521
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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