A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569017



Internal ID16009740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34430431..34470157hg38UCSC Ensembl
Innerchr15:34722632..34762358hg19UCSC Ensembl
Innerchr15:32509924..32549650hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3839727
hg1939727
hg1839727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4469n54
Supporting Variantsnssv840049, nssv840050
Samples
Known GenesGOLGA8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569017
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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