A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576578



Internal ID16363987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26169974..26184525hg38UCSC Ensembl
Innerchr18:23749938..23764489hg19UCSC Ensembl
Innerchr18:22003936..22018487hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3814552
hg1914552
hg1814552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878501
Samples
Known GenesPSMA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576578
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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