A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731413



Internal ID20507334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156582107..156582170hg38UCSC Ensembl
chr7:156374801..156374864hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288926
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731413
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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