A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045626



Internal ID19134845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179274..32283629hg38UCSC Ensembl
Innerchr15:32471475..32575830hg19UCSC Ensembl
Innerchr15:30258767..30363122hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38104356
hg19104356
hg18104356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2539n100
Supporting Variantsnssv3721630
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)nsv1045626
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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