A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041825



Internal ID19131044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42954840..42992538hg38UCSC Ensembl
Innerchr10:43450288..43487986hg19UCSC Ensembl
Innerchr10:42770294..42807992hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3837699
hg1937699
hg1837699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv722n100
Supporting Variantsnssv3508695
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)nsv1041825
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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