A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135796



Internal ID21454720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120006967..120006967hg38UCSC Ensembl
chr4:120928122..120928122hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610191
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135796
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