A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576442



Internal ID16363851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9205246..9206213hg38UCSC Ensembl
Innerchr18:9205244..9206211hg19UCSC Ensembl
Innerchr18:9195244..9196211hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38968
hg19968
hg18968
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5846n54
Supporting Variantsnssv878053
Samples
Known GenesANKRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576442
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