A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042775



Internal ID19131994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:84002158..84016279hg38UCSC Ensembl
Innerchr10:85761914..85776035hg19UCSC Ensembl
Innerchr10:85751894..85766015hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3814122
hg1914122
hg1814122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv946n100
Supporting Variantsnssv3512561
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)nsv1042775
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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