A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515681



Internal ID15096288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45352886..45364001hg38UCSC Ensembl
Innerchr19:45856144..45867259hg19UCSC Ensembl
Innerchr19:50547984..50559099hg18UCSC Ensembl
Innerchr19:50547984..50559099hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3811116
hg1911116
hg1811116
hg1711116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664367, nssv686357, nssv675988
Samples
Known GenesERCC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515681
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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