A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569924



Internal ID16010647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72094008..72094364hg38UCSC Ensembl
Innerchr15:72386349..72386705hg19UCSC Ensembl
Innerchr15:70173403..70173759hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38357
hg19357
hg18357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv844986, nssv844972, nssv844981, nssv844973, nssv844978, nssv844987, nssv844984, nssv844990, nssv844976, nssv844982, nssv844985, nssv844974, nssv844989, nssv844971, nssv844977, nssv844975, nssv844970, nssv844979, nssv844988, nssv844983, nssv844980
Samples
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569924
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer