A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6239951



Internal ID22044561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155805732..155805732hg38UCSC Ensembl
chr7:155598426..155598426hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17839519
Samples
Known GenesSHH
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6239951
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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