A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527874



Internal ID15108481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226370177..226375078hg38UCSC Ensembl
Innerchr1:226557878..226562779hg19UCSC Ensembl
Innerchr1:224624501..224629402hg18UCSC Ensembl
Innerchr1:222864613..222869514hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg384902
hg194902
hg184902
hg174902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704373
Samples
Known GenesPARP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527874
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