A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576547



Internal ID16363956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15047754..15221737hg38UCSC Ensembl
Innerchr18:15047753..15221736hg19UCSC Ensembl
Innerchr18:15037753..15211736hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38173984
hg19173984
hg18173984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5868n54
Supporting Variantsnssv878469, nssv878470
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576547
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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