A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569376



Internal ID16010099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49253235..49254741hg38UCSC Ensembl
Innerchr15:49545432..49546938hg19UCSC Ensembl
Innerchr15:47332724..47334230hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381507
hg191507
hg181507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4523n54
Supporting Variantsnssv842931, nssv842932
Samples
Known GenesGALK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569376
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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