A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569824



Internal ID16357233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71183376..71185419hg38UCSC Ensembl
Innerchr15:71475715..71477758hg19UCSC Ensembl
Innerchr15:69262769..69264812hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382044
hg192044
hg182044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4587n54
Supporting Variantsnssv844383, nssv844381, nssv844382
Samples
Known GenesTHSD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569824
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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