A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046276



Internal ID18788807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46553382..46592975hg38UCSC Ensembl
Innerchr10:46956642..46996235hg19UCSC Ensembl
Innerchr10:46376648..46416241hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3839594
hg1939594
hg1839594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv768n100
Supporting Variantsnssv3512769
Samples
Known GenesGPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046276
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