A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048716



Internal ID18791247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127524465..127552592hg38UCSC Ensembl
Innerchr10:129322729..129350856hg19UCSC Ensembl
Innerchr10:129212719..129240846hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3828128
hg1928128
hg1828128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518389
Samples
Known GenesNPS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048716
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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