A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074704



Internal ID21983937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24686052..24686052hg38UCSC Ensembl
chr7:24725671..24725671hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570857
Samples
Known GenesMPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074704
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