A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020439



Internal ID21929782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7182099..7188447hg38UCSC Ensembl
chr10:7224061..7230409hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386349
hg196349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593885
Samples
Known GenesSFMBT2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020439
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