A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154569



Internal ID21504096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126635238..126635238hg38UCSC Ensembl
chr7:126275292..126275292hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg386732
hg196732
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629477
Supporting Variants
SamplesNA19239
Known GenesGRM8
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154569
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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