A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038443



Internal ID18780974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23619450..23658140hg38UCSC Ensembl
Innerchr15:23864597..23903287hg19UCSC Ensembl
Innerchr15:21415690..21454380hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3838691
hg1938691
hg1838691
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3538886
Samples
Known GenesMAGEL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038443
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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