A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698089



Internal ID15088055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48673773..48693829hg38UCSC Ensembl
Innerchr19:49177030..49197086hg19UCSC Ensembl
Innerchr19:53868842..53888898hg18UCSC Ensembl
Innerchr19:53868842..53888898hg17UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3820057
hg1920057
hg1820057
hg1720057
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521477
Supporting Variants
Samples
Known GenesSEC1P
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698089
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer