A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150009



Internal ID15528237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69836..1506323hg38UCSC Ensembl
Innerchr18:69836..1506324hg19UCSC Ensembl
Innerchr18:59836..1496324hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg381436488
hg191436489
hg181436489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576228
Supporting Variants
SamplesHGDP00609
Known GenesADCYAP1, C18orf56, CETN1, CLUL1, COLEC12, ENOSF1, LINC00470, MIR8078, ROCK1P1, THOC1, TYMS, USP14, YES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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