A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14334649



Internal ID22126714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32566018..32566334hg38UCSC Ensembl
chr7:32605630..32605946hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3194855
Supporting Variants
SamplesHG00512
Known GenesAVL9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14334649
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