A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569928



Internal ID16010651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094008..72095726hg38UCSC Ensembl
Innerchr15:72386349..72388067hg19UCSC Ensembl
Innerchr15:70173403..70175121hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381719
hg191719
hg181719
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845019, nssv845004, nssv845009, nssv845027, nssv845014, nssv845045, nssv845026, nssv845022, nssv845034, nssv845037, nssv845031, nssv845029, nssv845008, nssv845010, nssv845006, nssv845016, nssv845012, nssv845043, nssv845021, nssv845030, nssv845044, nssv845020, nssv845039, nssv845007, nssv845024, nssv845040, nssv845033, nssv845005, nssv845025, nssv845035, nssv845015, nssv845036, nssv845017, nssv845018, nssv845023, nssv845003, nssv845046, nssv845038, nssv845041, nssv845011, nssv845028, nssv845042, nssv845032, nssv845013
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569928
Frequency
Sample Size17421
Observed Gain31
Observed Loss13
Observed Complex0
Frequencyn/a


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