A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886249



Internal ID16180205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:66696064..66778274hg38UCSC Ensembl
Innerchr18:64363301..64445511hg19UCSC Ensembl
Innerchr18:62514281..62596491hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3882211
hg1982211
hg1882211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577283
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)nssv886249
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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