A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039841



Internal ID19129060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52065251..52089180hg38UCSC Ensembl
Innerchr15:52357448..52381377hg19UCSC Ensembl
Innerchr15:50144740..50168669hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3823930
hg1923930
hg1823930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552402
Samples
Known GenesMAPK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039841
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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