A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765996



Internal ID22100468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136302172..136307357hg38UCSC Ensembl
chr3:136021014..136026199hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385186
hg195186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444413
Supporting Variants
Samples
Known GenesPCCB
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=SUBSDEL
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765996
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