A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437239



Internal ID22103417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5206163..5206358hg38UCSC Ensembl
chr17:5109458..5109653hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767208
Samples
Known GenesLOC100130950
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437239
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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