A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887250



Internal ID16181206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71335855..71381576hg38UCSC Ensembl
Innerchr18:69003091..69048812hg19UCSC Ensembl
Innerchr18:67154071..67199792hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3845722
hg1945722
hg1845722
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577587
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)nssv887250
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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