A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047376



Internal ID19136595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46574569..46595134hg38UCSC Ensembl
Innerchr10:46954483..46975048hg19UCSC Ensembl
Innerchr10:46374489..46395054hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3820566
hg1920566
hg1820566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518550
Samples
Known GenesSYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047376
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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