A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038894



Internal ID19128113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41745954..41785254hg38UCSC Ensembl
Innerchr15:42038152..42077452hg19UCSC Ensembl
Innerchr15:39825444..39864744hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3839301
hg1939301
hg1839301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552265
Samples
Known GenesMAPKBP1, MGA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038894
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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