A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040726



Internal ID18783257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133282503..133353665hg38UCSC Ensembl
Innerchr10:135096007..135167169hg19UCSC Ensembl
Innerchr10:134945997..135017159hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3871163
hg1971163
hg1871163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513503, nssv3515091
Samples
Known GenesCALY, PRAP1, TUBGCP2, ZNF511
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040726
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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