A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767685



Internal ID20543545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156655795..156655795hg38UCSC Ensembl
chr7:156448489..156448489hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285967
Samples
Known GenesRNF32
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767685
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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