A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570189



Internal ID16357598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77819044..77820182hg38UCSC Ensembl
Innerchr15:78111386..78112524hg19UCSC Ensembl
Innerchr15:75898441..75899579hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381139
hg191139
hg181139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4669n54
Supporting Variantsnssv847417, nssv847414, nssv847415, nssv847416, nssv847413
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570189
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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