A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569758



Internal ID16357167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65524895..65530103hg38UCSC Ensembl
Innerchr15:65817233..65822441hg19UCSC Ensembl
Innerchr15:63604286..63609494hg18UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385209
hg195209
hg185209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4577n54
Supporting Variantsnssv844190, nssv844189, nssv844188
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569758
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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