A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150590



Internal ID15532789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10487446..10515297hg38UCSC Ensembl
Innerchr18:10487443..10515294hg19UCSC Ensembl
Innerchr18:10477443..10505294hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3827852
hg1927852
hg1827852
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576476
Supporting Variants
SamplesHGDP01372
Known GenesAPCDD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150590
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