A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569542



Internal ID16356951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55893064..55918731hg38UCSC Ensembl
Innerchr15:56185262..56210929hg19UCSC Ensembl
Innerchr15:53972554..53998221hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3825668
hg1925668
hg1825668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843418
Samples
Known GenesNEDD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569542
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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