A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077537



Internal ID21986770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97132475..97132475hg38UCSC Ensembl
chr7:96761787..96761787hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566048
Samples
Known GenesACN9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077537
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