A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640156



Internal ID21588461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174382770..174382770hg38UCSC Ensembl
chr4:175303921..175303921hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124167
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640156
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