A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767759



Internal ID22102230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38217038..38217194hg38UCSC Ensembl
chr22:38613045..38613201hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4442091
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767759
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