A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515548



Internal ID15096155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28275803..28291040hg38UCSC Ensembl
Innerchr10:28564732..28579969hg19UCSC Ensembl
Innerchr10:28604738..28619975hg18UCSC Ensembl
Innerchr10:28604738..28619975hg17UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3815238
hg1915238
hg1815238
hg1715238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692794, nssv681776, nssv671218, nssv675278, nssv689015, nssv664059, nssv687437, nssv667241, nssv677353, nssv693090, nssv671042, nssv655380, nssv675537, nssv663877, nssv689794, nssv669862, nssv686096
Samples
Known GenesMIR8086, MPP7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515548
Frequency
Sample Size2026
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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