A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335548



Internal ID22301660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98049529..98049678hg38UCSC Ensembl
chr7:97678841..97678990hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527633
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335548
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