A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517624



Internal ID15444917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70551638..70555458hg38UCSC Ensembl
Innerchr10:72311394..72315214hg19UCSC Ensembl
Innerchr10:71981400..71985220hg18UCSC Ensembl
Innerchr10:71981400..71985220hg17UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383821
hg193821
hg183821
hg173821
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652572, nssv667460, nssv657410, nssv685957, nssv680905, nssv665660
Samples
Known GenesPALD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517624
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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