A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632609



Internal ID21580914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37683951..37683951hg38UCSC Ensembl
chr7:37723554..37723554hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145501
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632609
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