A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14337044



Internal ID22219856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140993580..140995333hg38UCSC Ensembl
chr7:140693380..140695133hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381754
hg191754
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527148
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14337044
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