A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045614



Internal ID19134833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27672432..27684909hg38UCSC Ensembl
Innerchr15:27917578..27930055hg19UCSC Ensembl
Innerchr15:25591173..25603650hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3812478
hg1912478
hg1812478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2488n100
Supporting Variantsnssv3545648
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)nsv1045614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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