A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15180026



Internal ID21318822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6977649..6977729hg38UCSC Ensembl
chr4:6979376..6979456hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3946945
Supporting Variants
SamplesHG002
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15180026
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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