A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071055



Internal ID21980288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87380337..87380337hg38UCSC Ensembl
chr7:87009653..87009653hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38147
hg19147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567529
Samples
Known GenesCROT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071055
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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