A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149599



Internal ID15533834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71969044..72010326hg38UCSC Ensembl
Innerchr15:72261385..72302667hg19UCSC Ensembl
Innerchr15:70048439..70089721hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3841283
hg1941283
hg1841283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569913
Supporting Variants
SamplesNINDS_222
Known GenesMYO9A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149599
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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