A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761823



Internal ID22096322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191694670..191694998hg38UCSC Ensembl
chr2:192559396..192559724hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SIMPLEDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761823
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