A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568300



Internal ID16355709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23323098..23416359hg38UCSC Ensembl
Innerchr15:23568239..23661506hg19UCSC Ensembl
Innerchr15:21119680..21212947hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3893262
hg1993268
hg1893268
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4331n54
Supporting Variantsnssv838446
Samples
Known GenesGOLGA8S, LOC440243
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568300
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