A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17852037



Internal ID22035680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7049198..7049198hg38UCSC Ensembl
chr3:7090885..7090885hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6253657
Supporting Variants
Samples
Known GenesGRM7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17852037
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