A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347770



Internal ID22122090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127464362..127464418hg38UCSC Ensembl
chr9:130226641..130226697hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217723
Supporting Variants
SamplesHG00512
Known GenesLRSAM1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347770
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