A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358984



Internal ID22196907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29183991..29184287hg38UCSC Ensembl
chr1:29510503..29510799hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525806
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358984
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