A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447648



Internal ID22113826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:78771163..78771252hg38UCSC Ensembl
chr8:79683398..79683487hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762854
Samples
Known GenesIL7
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SUBSDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447648
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer