A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14333085



Internal ID22326828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23504186..23505586hg38UCSC Ensembl
chr7:23543805..23545205hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381401
hg191401
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192781
Supporting Variants
SamplesNA19240
Known GenesTRA2A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14333085
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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