A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5577371



Internal ID21525823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6097832..6099455hg38UCSC Ensembl
chr7:6137463..6139086hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg381624
hg191624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140132
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5577371
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer