A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038377



Internal ID19127596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28666612..28689598hg38UCSC Ensembl
Innerchr15:28911758..28934744hg19UCSC Ensembl
Innerchr15:26710799..26733785hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3822987
hg1922987
hg1822987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545672
Samples
Known GenesHERC2P9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038377
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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