A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053127



Internal ID19142346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26340886..26376082hg38UCSC Ensembl
Innerchr15:26586033..26621229hg19UCSC Ensembl
Innerchr15:24137126..24172322hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3835197
hg1935197
hg1835197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545632
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)nsv1053127
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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