A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053665



Internal ID18796196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34893474..35230186hg38UCSC Ensembl
Innerchr10:35182402..35519114hg19UCSC Ensembl
Innerchr10:35222408..35559120hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38336713
hg19336713
hg18336713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv706n100
Supporting Variantsnssv3520117
Samples
Known GenesCREM, CUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053665
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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