A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012106



Internal ID21921449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75932784..75932896hg38UCSC Ensembl
chr7:75562102..75562214hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561033
Samples
Known GenesPOR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012106
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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