A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633264



Internal ID21581569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157042449..157042449hg38UCSC Ensembl
chr7:156835143..156835143hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143865
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633264
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