A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156518



Internal ID21457143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1089920..1089920hg38UCSC Ensembl
chr7:1129556..1129556hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640263
Supporting Variants
SamplesHG02587
Known GenesC7orf50, GPER1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156518
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