A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16289263



Internal ID20498481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156836745..156836797hg38UCSC Ensembl
chr1:156806537..156806589hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742656
Supporting Variants
Samples
Known GenesNTRK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16289263
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