A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568235



Internal ID16008958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22576506..23117883hg38UCSC Ensembl
Innerchr15:22755185..23296590hg19UCSC Ensembl
Innerchr15:20306549..20848031hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38541378
hg19541406
hg18541483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv838360
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568235
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