A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054568



Internal ID19143787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:109373130..109413797hg38UCSC Ensembl
Innerchr10:111132888..111173555hg19UCSC Ensembl
Innerchr10:111122878..111163545hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3840668
hg1940668
hg1840668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522676
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054568
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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