A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042534



Internal ID18785065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34933185..35208503hg38UCSC Ensembl
Innerchr10:35222113..35497431hg19UCSC Ensembl
Innerchr10:35262119..35537437hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38275319
hg19275319
hg18275319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv706n100
Supporting Variantsnssv3511202
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)nsv1042534
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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