A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576645



Internal ID16364054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:33803925..33840046hg38UCSC Ensembl
Innerchr18:31383889..31420010hg19UCSC Ensembl
Innerchr18:29637887..29674008hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3836122
hg1936122
hg1836122
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5884n54
Supporting Variantsnssv1150240
Samples1780862345_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576645
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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