A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv844968



Internal ID15792238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72093834..72095726hg38UCSC Ensembl
Innerchr15:72386175..72388067hg19UCSC Ensembl
Innerchr15:70173229..70175121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381893
hg191893
hg181893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569923
Supporting Variants
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv844968
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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