A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036324



Internal ID19125543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133451264..133515188hg38UCSC Ensembl
Innerchr10:135264768..135328692hg19UCSC Ensembl
Innerchr10:135114758..135178682hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3863925
hg1963925
hg1863925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1005n100
Supporting Variantsnssv3502821
Samples
Known GenesSCART1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036324
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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