A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053560



Internal ID19142779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24554857..24574091hg38UCSC Ensembl
Innerchr10:24843786..24863020hg19UCSC Ensembl
Innerchr10:24883792..24903026hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3819235
hg1919235
hg1819235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv693n100
Supporting Variantsnssv3522622
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)nsv1053560
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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