A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049432



Internal ID19138651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20501155..20533677hg38UCSC Ensembl
Innerchr10:20790084..20822606hg19UCSC Ensembl
Innerchr10:20830090..20862612hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3832523
hg1932523
hg1832523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv687n100
Supporting Variantsnssv3519729, nssv3707715
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)nsv1049432
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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