A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443837



Internal ID22110018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27380689..27380739hg38UCSC Ensembl
chr6:27348468..27348518hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767648
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443837
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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