A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446216



Internal ID22112395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163611643..163611711hg38UCSC Ensembl
chr6:164032675..164032743hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756564
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446216
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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