A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576558



Internal ID16363967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15390016..15405340hg38UCSC Ensembl
Innerchr18:15390015..15405339hg19UCSC Ensembl
Innerchr18:15380015..15395339hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3815325
hg1915325
hg1815325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5871n54
Supporting Variantsnssv878483
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576558
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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