A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036832



Internal ID19126051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38619590..38780907hg38UCSC Ensembl
Innerchr10:38912721..39074038hg19UCSC Ensembl
Innerchr10:38952727..39114044hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38161318
hg19161318
hg18161318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv710n100
Supporting Variantsnssv3518637, nssv3504110
Samples
Known GenesACTR3BP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036832
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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