A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439850



Internal ID22106027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69626119..69626236hg38UCSC Ensembl
chr8:70538354..70538471hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15764383
Samples
Known GenesSULF1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439850
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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