A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576434



Internal ID16017157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8705082..8706635hg38UCSC Ensembl
Innerchr18:8705080..8706633hg19UCSC Ensembl
Innerchr18:8695080..8696633hg18UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381554
hg191554
hg181554
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv878036, nssv878034, nssv878035, nssv878033
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576434
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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