A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053144



Internal ID18795675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34884759..35021379hg38UCSC Ensembl
Innerchr10:35173687..35310307hg19UCSC Ensembl
Innerchr10:35213693..35350313hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38136621
hg19136621
hg18136621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv705n100
Supporting Variantsnssv3521551
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)nsv1053144
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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