A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053276



Internal ID19142495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27585641..27605433hg38UCSC Ensembl
Innerchr15:27830787..27850579hg19UCSC Ensembl
Innerchr15:25504382..25524174hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3819793
hg1919793
hg1819793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3545635
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)nsv1053276
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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