A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576553



Internal ID16363962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15199708..15290107hg38UCSC Ensembl
Innerchr18:15199707..15290106hg19UCSC Ensembl
Innerchr18:15189707..15280106hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3890400
hg1990400
hg1890400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5869n54
Supporting Variantsnssv878477
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576553
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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