A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435987



Internal ID22493857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111869716..111869716hg38UCSC Ensembl
chr7:111509772..111509772hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961056
Supporting Variants
Samples
Known GenesDOCK4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435987
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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