A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044158



Internal ID19133377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58080408..58120472hg38UCSC Ensembl
Innerchr10:59840168..59880233hg19UCSC Ensembl
Innerchr10:59510174..59550239hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3840065
hg1940066
hg1840066
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv877n100
Supporting Variantsnssv3513942
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)nsv1044158
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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