A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049394



Internal ID18791925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46526932..46602921hg38UCSC Ensembl
Innerchr10:46946696..47022685hg19UCSC Ensembl
Innerchr10:46366702..46442691hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3875990
hg1975990
hg1875990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515917
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)nsv1049394
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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