A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042764



Internal ID18785295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42350935..43016264hg38UCSC Ensembl
Innerchr10:42846383..43511712hg19UCSC Ensembl
Innerchr10:42166389..42831718hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38665330
hg19665330
hg18665330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3512555
Samples
Known GenesBMS1, CCNYL2, LINC00839, LOC441666, MIR5100, ZNF33B, ZNF37BP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042764
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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