A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040684



Internal ID19129903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87462181..87507820hg38UCSC Ensembl
Innerchr15:88005412..88051051hg19UCSC Ensembl
Innerchr15:85806416..85852055hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3845640
hg1945640
hg1845640
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555192
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040684
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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