A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050824



Internal ID19140043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58075195..58136187hg38UCSC Ensembl
Innerchr10:59834955..59895948hg19UCSC Ensembl
Innerchr10:59504961..59565954hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3860993
hg1960994
hg1860994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv876n100
Supporting Variantsnssv3517358
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)nsv1050824
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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