A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041642



Internal ID19130861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27674339..27687762hg38UCSC Ensembl
Innerchr15:27919485..27932908hg19UCSC Ensembl
Innerchr15:25593080..25606503hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3813424
hg1913424
hg1813424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2488n100
Supporting Variantsnssv3545655, nssv3545657, nssv3545656
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)nsv1041642
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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