A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446248



Internal ID22112427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87941590..87941662hg38UCSC Ensembl
chr6:88651308..88651380hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758561
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446248
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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