A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878485



Internal ID16172441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15394867..15406657hg38UCSC Ensembl
Innerchr18:15394866..15406656hg19UCSC Ensembl
Innerchr18:15384866..15396656hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3811791
hg1911791
hg1811791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576560
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878485
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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