A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984798



Internal ID21894141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66735533..66735862hg38UCSC Ensembl
chr1:67201216..67201545hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525004
Samples
Known GenesSGIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984798
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