A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205050



Internal ID22353806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92227743..92228131hg38UCSC Ensembl
chr7:91857057..91857445hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14336062, nssv14336063
SamplesHG00731, HG00733
Known GenesKRIT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205050
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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