A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051087



Internal ID18793618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49977683..50687535hg38UCSC Ensembl
Innerchr10:51737443..52447295hg19UCSC Ensembl
Innerchr10:51407449..52117301hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38709853
hg19709853
hg18709853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706904
Samples
Known GenesAGAP6, ASAH2, FAM21A, FAM21B, FLJ31813, SGMS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051087
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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