A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576437



Internal ID16363846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8705170..8706759hg38UCSC Ensembl
Innerchr18:8705168..8706757hg19UCSC Ensembl
Innerchr18:8695168..8696757hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381590
hg191590
hg181590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5845n54
Supporting Variantsnssv878045, nssv878044
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576437
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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