A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001102



Internal ID21910445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176607745..176607801hg38UCSC Ensembl
chr5:176034746..176034802hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566646
Samples
Known GenesGPRIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001102
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