A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15756777



Internal ID22091250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:10507910..10507961hg38UCSC Ensembl
chr3:10549594..10549645hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445521
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15756777
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