A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037134



Internal ID18779665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34871114..35045560hg38UCSC Ensembl
Innerchr10:35160042..35334488hg19UCSC Ensembl
Innerchr10:35200048..35374494hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38174447
hg19174447
hg18174447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv705n100
Supporting Variantsnssv3504724
Samples
Known GenesCUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037134
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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