A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038080



Internal ID18780611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29361590..29565510hg38UCSC Ensembl
Innerchr10:29650519..29854439hg19UCSC Ensembl
Innerchr10:29690525..29894445hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38203921
hg19203921
hg18203921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707747
Samples
Known GenesMIR604, PTCHD3P1, SVIL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038080
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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