A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149600



Internal ID15533849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71969044..72033254hg38UCSC Ensembl
Innerchr15:72261385..72325595hg19UCSC Ensembl
Innerchr15:70048439..70112649hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3864211
hg1964211
hg1864211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569914
Supporting Variants
SamplesNINDS_223
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149600
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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