A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051775



Internal ID19140994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46467768..46489856hg38UCSC Ensembl
Innerchr10:47055642..47081683hg19UCSC Ensembl
Innerchr10:46475648..46501689hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3822089
hg1926042
hg1826042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv805n100
Supporting Variantsnssv3520056, nssv3522152
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)nsv1051775
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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