A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525448



Internal ID15106055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28048641..28274803hg38UCSC Ensembl
Innerchr10:28337570..28563732hg19UCSC Ensembl
Innerchr10:28377576..28603738hg18UCSC Ensembl
Innerchr10:28377576..28603738hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38226163
hg19226163
hg18226163
hg17226163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701576
Samples
Known GenesMPP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525448
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