A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050351



Internal ID19139570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130376713..130491930hg38UCSC Ensembl
Innerchr10:132174977..132290194hg19UCSC Ensembl
Innerchr10:132064967..132180184hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38115218
hg19115218
hg18115218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520788
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)nsv1050351
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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