A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528555



Internal ID15109162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95311275..95329316hg38UCSC Ensembl
Innerchr7:94940587..94958628hg19UCSC Ensembl
Innerchr7:94778523..94796564hg18UCSC Ensembl
Innerchr7:94585238..94603279hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3818042
hg1918042
hg1818042
hg1718042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705169
Samples
Known GenesPON1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528555
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